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Most recent job postings at ucb
via UCB Careers
schedule_type: Full-time
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Product Information – Regulatory Affairs group, based in our Smyrna, GA offices, we are looking for a talented individual to fill the position of: Regulatory Labeling, Advertising and Promotion Scientist.
The Regulatory Labeling, Advertising and Promotion Scientist act as regulatory approver of all advertising and promotional materials and take an active role in submission of these materials to the FDA.
You like to work in an environment where you can:
• Operate as the regulatory representative to the cross functional team creating the advertising and promotional materials, bring product knowledge, information on previous submissions, FDA enforcement trends, and the competitive landscape to all discussions.
• Lead development of new labeling content in collaboration with cross functional project team.
• Manage the creation and maintenance of all US product labeling components using the established labeling and artwork procedures in collaboration with the Regulatory Labeling, Advertising and Promotion Scientist Lead.
• Compile labeling documents for all submissions which include labeling information.
• Take charge for drug listing for product manufactured by UCB for distribution within the US.
• Develop and maintain current knowledge of requirements for US regulation of drug marketing and advertising and competitive landscape.
• Communicate FDA requirements to other UCB departments involved in the preparation or review of external communication materials.
• Collaborate with co-creation partners in the development of new promotional initiatives/programs and reviews supporting materials ensuring compliance and consistency with internal policies, Code of Federal Regulations (CFR), FDA guidance documents, PhRMA Guiding Principles, and the Federal Food, Drug, and Cosmetic Act.
• Negotiates promotional regulatory position within cross-functional team.
• Works on complex OPDP submissions in collaboration with Regulatory Labeling, Advertising and Promotion Manager, US.
• Participate in and/or directs the regulatory review of non-promotional scientific information, and external communication materials, including media information and provides proactive feedback.
You will contribute by:
• Developing and maintaining current knowledge of US regulation of labeling and industry standards for labeling and communicate requirements to other departments in a timely manner.
• Directing the labeling control process for tracking, implementation, and regulatory submission of changes to existing labeling.
• Interfacing with the Global Labeling Function (GLF) to ensure consistency of labeling processes and local compliance with CCDS.
• Compiling Labeling Review Committee (LRC) packages for all US labeling components.
• Managing LRC and GLF reviews and approvals.
• Managing artwork revisions to US labeling components using the established artwork processes.
• Compiling labeling documents required for all FDA submissions which include labeling information.
• Maintaining drug product listings.
• Managing generation of SPL for inclusion in labeling submissions and drug product listings.
• Collaborating with Supply Chain to coordinate implementation strategy for new labeling artwork components.
Interested? For this position, you’ll need the following education, experience, and skills:
Minimum Qualifications:
• BSc with 3+ years of relevant experience in the pharmaceutical industry.
• 2+ years in Regulatory Affairs and specific experience in US advertising and promotion material review, approval and labeling.
• Demonstrated knowledge of US labeling and promotion regulations and guidance.
• Thorough knowledge of science and data of assigned products and how that translates into labeling language.
• Proven track record of competitive landscape and how other companies are dealing with similar issues in labeling and promotion.
• Demonstrated experience of product launch within previous organizations.
RANDATUCB
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Product Information – Regulatory Affairs group, based in our Smyrna, GA offices, we are looking for a talented individual to fill the position of: Regulatory Labeling, Advertising and Promotion Scientist.
The Regulatory Labeling, Advertising and Promotion Scientist act as regulatory approver of all advertising and promotional materials and take an active role in submission of these materials to the FDA.
You like to work in an environment where you can:
• Operate as the regulatory representative to the cross functional team creating the advertising and promotional materials, bring product knowledge, information on previous submissions, FDA enforcement trends, and the competitive landscape to all discussions.
• Lead development of new labeling content in collaboration with cross functional project team.
• Manage the creation and maintenance of all US product labeling components using the established labeling and artwork procedures in collaboration with the Regulatory Labeling, Advertising and Promotion Scientist Lead.
• Compile labeling documents for all submissions which include labeling information.
• Take charge for drug listing for product manufactured by UCB for distribution within the US.
• Develop and maintain current knowledge of requirements for US regulation of drug marketing and advertising and competitive landscape.
• Communicate FDA requirements to other UCB departments involved in the preparation or review of external communication materials.
• Collaborate with co-creation partners in the development of new promotional initiatives/programs and reviews supporting materials ensuring compliance and consistency with internal policies, Code of Federal Regulations (CFR), FDA guidance documents, PhRMA Guiding Principles, and the Federal Food, Drug, and Cosmetic Act.
• Negotiates promotional regulatory position within cross-functional team.
• Works on complex OPDP submissions in collaboration with Regulatory Labeling, Advertising and Promotion Manager, US.
• Participate in and/or directs the regulatory review of non-promotional scientific information, and external communication materials, including media information and provides proactive feedback.
You will contribute by:
• Developing and maintaining current knowledge of US regulation of labeling and industry standards for labeling and communicate requirements to other departments in a timely manner.
• Directing the labeling control process for tracking, implementation, and regulatory submission of changes to existing labeling.
• Interfacing with the Global Labeling Function (GLF) to ensure consistency of labeling processes and local compliance with CCDS.
• Compiling Labeling Review Committee (LRC) packages for all US labeling components.
• Managing LRC and GLF reviews and approvals.
• Managing artwork revisions to US labeling components using the established artwork processes.
• Compiling labeling documents required for all FDA submissions which include labeling information.
• Maintaining drug product listings.
• Managing generation of SPL for inclusion in labeling submissions and drug product listings.
• Collaborating with Supply Chain to coordinate implementation strategy for new labeling artwork components.
Interested? For this position, you’ll need the following education, experience, and skills:
Minimum Qualifications:
• BSc with 3+ years of relevant experience in the pharmaceutical industry.
• 2+ years in Regulatory Affairs and specific experience in US advertising and promotion material review, approval and labeling.
• Demonstrated knowledge of US labeling and promotion regulations and guidance.
• Thorough knowledge of science and data of assigned products and how that translates into labeling language.
• Proven track record of competitive landscape and how other companies are dealing with similar issues in labeling and promotion.
• Demonstrated experience of product launch within previous organizations.
RANDATUCB
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
via UCB Careers
schedule_type: Full-time
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better. At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives... of patients. We promote an environment of
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better. At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives... of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions. An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Neurology Missions team in the Great Lakes region, we are looking for a talented individual to fill the position of: Medical Science Liaison - (Neuromuscular & Autoimmune Disease).
The Medical Science Liaison (MSL) provides peer-level scientific exchange with clinicians and researchers working in neuromuscular and autoimmune diseases at UCB. This individual develops relationships of trust and mutual support built on common interests in fostering deep, science driven understanding of auto-immune diseases such as myasthenia gravis, advancing potential new therapies, and mapping new strategies for patient value creation. This position covers the Great Lakes region of the United States which includes Ohio, Michigan, and West Virginia.
You like to work in an environment where you can:
• Play a crucial role in the development of the rare disease MSL organization
• Manage and execute stakeholder engagement within a local region based on training, expertise, and individualized approaches to identifying local needs and opportunities
• Engage regularly with: clinical trial sites, investigators, key opinion leaders, and patient advocacy organizations with the common goal of seeking to improve the lives of patients with rare diseases
• Provide training and expertise to internal colleagues as a subject matter expert within selected disorders with a focus on FcRn and complement physiology and pathophysiology
You will contribute by:
• Fostering appropriate discussion of UCB research objectives and findings through thought leader engagement and educational activities
• Representing UCB at local, regional, and national professional and academic conferences where issues related to the diagnosis and treatment of myasthenia gravis and related autoimmune disorders are addressed
• Mapping existing care pathways in myasthenia gravis within his/her area to identify unique or evolving unmet patient needs
• Identifying and cultivating potential clinical trial partners and working with existing trial sites to ensure recruitment, participation and reporting objectives are met and are compliant with UCB standards of practice
• Developing relationships with leading academic researchers and KOLs thought leaders to achieve alignment on key research and clinical objectives
Interested? For this position, you'll need the following education, experience, and skills:
Minimum Qualifications:
• PharmD, PHD and MD
• 3 + years of Medical Science Liaison experience for an orphan disease drug or biotherapeutic
• Valid Driver's License
Preferred Qualifications:
• Working experience in neuromuscular and/or autoimmune diseases preferred
• Excellent communication and presentation skills
• Ability to clearly articulate complex scientific concepts in 1:1 and group settings
• Strong desire and ability to be proactive, identify areas of opportunity, and consistently execute
About us:
At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.
With a team of approximately 7,600 employees and worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decision makers across the heath care ecosystem.
Curious to know more? Please visit our website www.ucb.com.
The Company is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, national origin, religion, gender, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.
Where permitted, applicants for employment in the United States must either have received or been willing to receive a full COVID-19 vaccination by the date of hire; or, alternatively, agree to be subject to weekly COVID-19 testing, subject to religious and medical exemptions and in accordance with applicable law Show more details...
We’re here because we want to build the future and transform patients’ lives for the better. At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives... of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions. An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Neurology Missions team in the Great Lakes region, we are looking for a talented individual to fill the position of: Medical Science Liaison - (Neuromuscular & Autoimmune Disease).
The Medical Science Liaison (MSL) provides peer-level scientific exchange with clinicians and researchers working in neuromuscular and autoimmune diseases at UCB. This individual develops relationships of trust and mutual support built on common interests in fostering deep, science driven understanding of auto-immune diseases such as myasthenia gravis, advancing potential new therapies, and mapping new strategies for patient value creation. This position covers the Great Lakes region of the United States which includes Ohio, Michigan, and West Virginia.
You like to work in an environment where you can:
• Play a crucial role in the development of the rare disease MSL organization
• Manage and execute stakeholder engagement within a local region based on training, expertise, and individualized approaches to identifying local needs and opportunities
• Engage regularly with: clinical trial sites, investigators, key opinion leaders, and patient advocacy organizations with the common goal of seeking to improve the lives of patients with rare diseases
• Provide training and expertise to internal colleagues as a subject matter expert within selected disorders with a focus on FcRn and complement physiology and pathophysiology
You will contribute by:
• Fostering appropriate discussion of UCB research objectives and findings through thought leader engagement and educational activities
• Representing UCB at local, regional, and national professional and academic conferences where issues related to the diagnosis and treatment of myasthenia gravis and related autoimmune disorders are addressed
• Mapping existing care pathways in myasthenia gravis within his/her area to identify unique or evolving unmet patient needs
• Identifying and cultivating potential clinical trial partners and working with existing trial sites to ensure recruitment, participation and reporting objectives are met and are compliant with UCB standards of practice
• Developing relationships with leading academic researchers and KOLs thought leaders to achieve alignment on key research and clinical objectives
Interested? For this position, you'll need the following education, experience, and skills:
Minimum Qualifications:
• PharmD, PHD and MD
• 3 + years of Medical Science Liaison experience for an orphan disease drug or biotherapeutic
• Valid Driver's License
Preferred Qualifications:
• Working experience in neuromuscular and/or autoimmune diseases preferred
• Excellent communication and presentation skills
• Ability to clearly articulate complex scientific concepts in 1:1 and group settings
• Strong desire and ability to be proactive, identify areas of opportunity, and consistently execute
About us:
At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.
With a team of approximately 7,600 employees and worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decision makers across the heath care ecosystem.
Curious to know more? Please visit our website www.ucb.com.
The Company is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, national origin, religion, gender, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.
Where permitted, applicants for employment in the United States must either have received or been willing to receive a full COVID-19 vaccination by the date of hire; or, alternatively, agree to be subject to weekly COVID-19 testing, subject to religious and medical exemptions and in accordance with applicable law Show more details...
via UCB Careers
schedule_type: Full-time
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Global Clinical Science & Operations (GCSO) department, based either in Monheim (Germany), Brussels (Belgium), Slough (UK) or Raleigh (US) we are looking for a talented individual to fill the position of: Head Clinical Data Standards
As Head of Clinical Data Standards you will be responsible for the development, maintenance and adherence to UCB’s clinical data standards including eCRF (forms, edit checks, controlled terminologies etc.,) data transfer agreements for clinical studies, SDTM and SDTM mappings. The role coordinates/contributes to wider Development Solutions data standards leadership and governance as well end-to-end automation of clinical data flow.
You like to work in an environment where you can:
• Oversee the development, maintenance and adherence to UCB’s clinical data standards and documentation
• Lead a global team managing standards and ensuring external intelligence and collaboration is incorporated into UCB’s practices
You will contribute by:
• Overseeing the process and technology used to store standards and automate the end to end clinical data flow
• Engaging internal and any external stakeholders to ensure awareness, understanding and alignment related to Data Standards and their associated benefits and processes/requirements/dependencies.
• Pro-actively engaging external forums to identify opportunities and best practices and standards to implement within UCB
• Supports efforts to integrate and harmonize activities across multiple sites with an emphasis on team spirit, work style, consistent processes and technology
Interested? For this position you’ll need the following education, experience and skills:
• Relevant academic background
• 10+ years of experience in a CRO/pharmaceutical environment with a proven and consistent record of proactive management and innovation
• 5+ years of experience in the CRO/pharmaceutical environment related to the development/implementation of (clinical) Data Standards, esp. CDISC
• 3+ years of line management experience in a CRO/pharmaceutical environment with a successful record of developing personnel and teams
• Thorough knowledge and understanding of standards development processes, esp. for clinical data
• Comprehensive knowledge of Standards Data Organizations (SDOs) and ability to utilize their resources to gain value for UCB
• Strong knowledge of CDISC, HL7, and ISO standards
• Exceptional communication skills in English (verbal and in writing)
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Global Clinical Science & Operations (GCSO) department, based either in Monheim (Germany), Brussels (Belgium), Slough (UK) or Raleigh (US) we are looking for a talented individual to fill the position of: Head Clinical Data Standards
As Head of Clinical Data Standards you will be responsible for the development, maintenance and adherence to UCB’s clinical data standards including eCRF (forms, edit checks, controlled terminologies etc.,) data transfer agreements for clinical studies, SDTM and SDTM mappings. The role coordinates/contributes to wider Development Solutions data standards leadership and governance as well end-to-end automation of clinical data flow.
You like to work in an environment where you can:
• Oversee the development, maintenance and adherence to UCB’s clinical data standards and documentation
• Lead a global team managing standards and ensuring external intelligence and collaboration is incorporated into UCB’s practices
You will contribute by:
• Overseeing the process and technology used to store standards and automate the end to end clinical data flow
• Engaging internal and any external stakeholders to ensure awareness, understanding and alignment related to Data Standards and their associated benefits and processes/requirements/dependencies.
• Pro-actively engaging external forums to identify opportunities and best practices and standards to implement within UCB
• Supports efforts to integrate and harmonize activities across multiple sites with an emphasis on team spirit, work style, consistent processes and technology
Interested? For this position you’ll need the following education, experience and skills:
• Relevant academic background
• 10+ years of experience in a CRO/pharmaceutical environment with a proven and consistent record of proactive management and innovation
• 5+ years of experience in the CRO/pharmaceutical environment related to the development/implementation of (clinical) Data Standards, esp. CDISC
• 3+ years of line management experience in a CRO/pharmaceutical environment with a successful record of developing personnel and teams
• Thorough knowledge and understanding of standards development processes, esp. for clinical data
• Comprehensive knowledge of Standards Data Organizations (SDOs) and ability to utilize their resources to gain value for UCB
• Strong knowledge of CDISC, HL7, and ISO standards
• Exceptional communication skills in English (verbal and in writing)
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
via UCB Careers
schedule_type: Full-time
Make your mark for patients
To strengthen our Rare Disease Global Medical Affairs team, we are looking for a talented individual to fill the position of: Global Rare Disease Scientific Communications Lead to be based in one of our hubs in Europe or from Atlanta / Boston...
With a great understanding of the innovative thinking process and a natural attitude in building and maintaining long-term trustable relationships, the Global Scientific Communications
Make your mark for patients
To strengthen our Rare Disease Global Medical Affairs team, we are looking for a talented individual to fill the position of: Global Rare Disease Scientific Communications Lead to be based in one of our hubs in Europe or from Atlanta / Boston...
With a great understanding of the innovative thinking process and a natural attitude in building and maintaining long-term trustable relationships, the Global Scientific Communications Lead is responsible for understanding the strategic needs and translate them into actionable medical scientific communications plans. Pragmatic and solution-oriented, they have a deep understanding of the different communications environments and channels along with their characteristics, nuances, and risks. In close alignment with GMIT (Global Medical Indication Team) and GRPT (Global Regional Program Team) the Global Medical Communications Lead is accountable for ensuring the key communications messages for the assigned asset(s) will reach the intended audiences in a timely manner and according to standards and regulations by means of the most appropriate tool and channel(s)
You like to work in an environment where you can:
• Lead and be accountable for effective and impactful medical/scientific communications planning and execution over the life cycle for the assigned asset(s) with adequate/minimal supervision, ensuring alignment to the Global Medical Strategy and the cross-functional teams within UCB
• Explore feasibility and advocate for innovative ideas to communicate assets’ key messages along with UCB values making standing UCB out
You will contribute by:
• Creating and fostering a culture of integrity, collaboration, shared ideas and of a forward-thinking environment
• Participating in Medical sub team meetings under the leadership of GMIL (Global Medical Indication Lead) to contribute to the development of Medical Strategy,
• Leading the Scientific Communications Strategy and consequently ensuring alignment of an integrated communications plan with the overall Medical Strategy.
• Liaising with Regional teams and ensuring that regional and local needs and plans are captured in a comprehensive strategy and plan
• Managing appropriately the allocated budget and prioritizing according to the needs of a fast-paced environment
• Periodically reporting on metrics on key objectives and on advancement of projects
• Manage assigned projects and oversee vendors to ensure development of scientifically accurate materials that aligns with the Scientific Communications Platform
Interested? For this position, you'll need the following education, experience and skills:
Qualifications:
• Master’s Degree in a scientific or medical discipline, Ph.D. or PharmD preferred
• 5-7 years overall experience in Medical Communications ideally in Neurology/ neuroinflammation/ neurodegenerative and/or genetic diseases, (rare or ultra-rare disease experience preferred), of which 4 gained working in a matrix organization (preferably in Medical Affairs, Medical Information, Field Medical, Scientific Communication agency)
• Excellent understanding of and ability to master traditional and modern communications techniques and channels, matched with excellent written and oral communication skills, including strong formal presentation skills
• Work efficiently with pragmatic approach to challenges, able to deal with agile frameworks and programs to deliver results that maximize patient value
• Skilled at promoting a culture of sharing and collaboration, able to efficiently control, and continuously adapt the project plan, with the appropriate level of details, to achieve the project objectives
• Maintains extensive knowledge of the relevant therapeutic areas, diseases, stakeholders, patient journeys and unmet needs, clinical practice, research and development, regulatory, market access environment, and the competitive landscape; applies this knowledge to develop differentiated patient solutions
• Successful track record of implementation of scientific communications programs
• Willingness/Ability to travel up to 30% at times is required
Why you should apply
At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact.
Through meaningful recognition and a challenging international work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve. Join us!
About UCB in Rare Diseases
We’re driven by patient value, not patient numbers.
People with rare diseases often feel forgotten, unheard or misunderstood. The challenges they face can be magnified by isolation, and they may wonder if anyone else cares about what they need. They worry their disease affects too few people for anybody to care.
The greatest needs can’t always be measured in numbers. At UCB, we don’t just see patients or population sizes, we see people in need. Through decades of serving the neurology and immunology communities, we have improved lives with impactful medicines and by enhancing the social and emotional well-being of patients. As a continuation of our heritage, and a progression of our science, we are expanding our efforts to developing treatments for rare neurological and immunologic diseases where current options offer little hope. We believe our scientific strength in these fields can create genuine value for the patient communities we serve.
Curious to know more? Please visit our website at www.ucb.com
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
Why work for us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
Learn more about sustainability at UCB and how it is integrated into our business approach.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
To strengthen our Rare Disease Global Medical Affairs team, we are looking for a talented individual to fill the position of: Global Rare Disease Scientific Communications Lead to be based in one of our hubs in Europe or from Atlanta / Boston...
With a great understanding of the innovative thinking process and a natural attitude in building and maintaining long-term trustable relationships, the Global Scientific Communications Lead is responsible for understanding the strategic needs and translate them into actionable medical scientific communications plans. Pragmatic and solution-oriented, they have a deep understanding of the different communications environments and channels along with their characteristics, nuances, and risks. In close alignment with GMIT (Global Medical Indication Team) and GRPT (Global Regional Program Team) the Global Medical Communications Lead is accountable for ensuring the key communications messages for the assigned asset(s) will reach the intended audiences in a timely manner and according to standards and regulations by means of the most appropriate tool and channel(s)
You like to work in an environment where you can:
• Lead and be accountable for effective and impactful medical/scientific communications planning and execution over the life cycle for the assigned asset(s) with adequate/minimal supervision, ensuring alignment to the Global Medical Strategy and the cross-functional teams within UCB
• Explore feasibility and advocate for innovative ideas to communicate assets’ key messages along with UCB values making standing UCB out
You will contribute by:
• Creating and fostering a culture of integrity, collaboration, shared ideas and of a forward-thinking environment
• Participating in Medical sub team meetings under the leadership of GMIL (Global Medical Indication Lead) to contribute to the development of Medical Strategy,
• Leading the Scientific Communications Strategy and consequently ensuring alignment of an integrated communications plan with the overall Medical Strategy.
• Liaising with Regional teams and ensuring that regional and local needs and plans are captured in a comprehensive strategy and plan
• Managing appropriately the allocated budget and prioritizing according to the needs of a fast-paced environment
• Periodically reporting on metrics on key objectives and on advancement of projects
• Manage assigned projects and oversee vendors to ensure development of scientifically accurate materials that aligns with the Scientific Communications Platform
Interested? For this position, you'll need the following education, experience and skills:
Qualifications:
• Master’s Degree in a scientific or medical discipline, Ph.D. or PharmD preferred
• 5-7 years overall experience in Medical Communications ideally in Neurology/ neuroinflammation/ neurodegenerative and/or genetic diseases, (rare or ultra-rare disease experience preferred), of which 4 gained working in a matrix organization (preferably in Medical Affairs, Medical Information, Field Medical, Scientific Communication agency)
• Excellent understanding of and ability to master traditional and modern communications techniques and channels, matched with excellent written and oral communication skills, including strong formal presentation skills
• Work efficiently with pragmatic approach to challenges, able to deal with agile frameworks and programs to deliver results that maximize patient value
• Skilled at promoting a culture of sharing and collaboration, able to efficiently control, and continuously adapt the project plan, with the appropriate level of details, to achieve the project objectives
• Maintains extensive knowledge of the relevant therapeutic areas, diseases, stakeholders, patient journeys and unmet needs, clinical practice, research and development, regulatory, market access environment, and the competitive landscape; applies this knowledge to develop differentiated patient solutions
• Successful track record of implementation of scientific communications programs
• Willingness/Ability to travel up to 30% at times is required
Why you should apply
At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact.
Through meaningful recognition and a challenging international work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve. Join us!
About UCB in Rare Diseases
We’re driven by patient value, not patient numbers.
People with rare diseases often feel forgotten, unheard or misunderstood. The challenges they face can be magnified by isolation, and they may wonder if anyone else cares about what they need. They worry their disease affects too few people for anybody to care.
The greatest needs can’t always be measured in numbers. At UCB, we don’t just see patients or population sizes, we see people in need. Through decades of serving the neurology and immunology communities, we have improved lives with impactful medicines and by enhancing the social and emotional well-being of patients. As a continuation of our heritage, and a progression of our science, we are expanding our efforts to developing treatments for rare neurological and immunologic diseases where current options offer little hope. We believe our scientific strength in these fields can create genuine value for the patient communities we serve.
Curious to know more? Please visit our website at www.ucb.com
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
Why work for us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
Learn more about sustainability at UCB and how it is integrated into our business approach.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
via UCB Careers
schedule_type: Full-time
Make your mark for patients
Regulatory Scientist US...
We are looking for an Expert Regulatory Scientist with flexibility and strong project management and communication skills to join our Regulatory Affairs team based in Raleigh, NC.
About the role:
• Support the Global Regulatory Scientist Lead for the delivery of timely approvals and product information in keeping with the needs identified by the business and markets and in compliance with
Make your mark for patients
Regulatory Scientist US...
We are looking for an Expert Regulatory Scientist with flexibility and strong project management and communication skills to join our Regulatory Affairs team based in Raleigh, NC.
About the role:
• Support the Global Regulatory Scientist Lead for the delivery of timely approvals and product information in keeping with the needs identified by the business and markets and in compliance with relevant UCB procedures and regional/local country regulations.
• Respect the planning, coordinate preparation and delivery of both simple and complex submissions throughout the product’s life cycle from either a global and/or regional perspective.
Who you’ll work with:
• Work flexibly within and across regions (US, Canada, EU, …) to provide broad operational support to ensure the delivery of product team and business objectives.
• Liaise proactively with the functions and participate as a member of cross- functional delivery teams for complex submissions, providing regulatory advice
• Assume assigned responsibilities for routine and non-routine contact with health authorities and affiliates to support the Global Regulatory Scientist Lead.
What you’ll do:
• Prepare and deliver regulatory operational plans for assigned projects/products within a specific region as agreed with the Regulatory Scientist Lead / Manager.
• Provide strategic and operational regulatory input and guidance in cross-functional teams.
• Provide regulatory expertise on regulatory submissions, health authority briefing documents and response documents
• Manage quality regulatory submissions to agreed project targets and assist in development of regulatory standards and SOPs / Workshops
• Identify potential regulatory risks to the operational plan, and propose options to mitigate risks.
Interested? For this role we’re looking for:
Bachelor’s degree with 3+ years of pharmaceutical industry experience.
Why you should apply:
At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
If you are interested to learn more about R&D within UCB, please find more information here R&D at UCB.
RANDATUCB
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
Why work for us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
Learn more about sustainability at UCB and how it is integrated into our business approach.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
Regulatory Scientist US...
We are looking for an Expert Regulatory Scientist with flexibility and strong project management and communication skills to join our Regulatory Affairs team based in Raleigh, NC.
About the role:
• Support the Global Regulatory Scientist Lead for the delivery of timely approvals and product information in keeping with the needs identified by the business and markets and in compliance with relevant UCB procedures and regional/local country regulations.
• Respect the planning, coordinate preparation and delivery of both simple and complex submissions throughout the product’s life cycle from either a global and/or regional perspective.
Who you’ll work with:
• Work flexibly within and across regions (US, Canada, EU, …) to provide broad operational support to ensure the delivery of product team and business objectives.
• Liaise proactively with the functions and participate as a member of cross- functional delivery teams for complex submissions, providing regulatory advice
• Assume assigned responsibilities for routine and non-routine contact with health authorities and affiliates to support the Global Regulatory Scientist Lead.
What you’ll do:
• Prepare and deliver regulatory operational plans for assigned projects/products within a specific region as agreed with the Regulatory Scientist Lead / Manager.
• Provide strategic and operational regulatory input and guidance in cross-functional teams.
• Provide regulatory expertise on regulatory submissions, health authority briefing documents and response documents
• Manage quality regulatory submissions to agreed project targets and assist in development of regulatory standards and SOPs / Workshops
• Identify potential regulatory risks to the operational plan, and propose options to mitigate risks.
Interested? For this role we’re looking for:
Bachelor’s degree with 3+ years of pharmaceutical industry experience.
Why you should apply:
At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
If you are interested to learn more about R&D within UCB, please find more information here R&D at UCB.
RANDATUCB
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
Why work for us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
Learn more about sustainability at UCB and how it is integrated into our business approach.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
via UCB Careers
schedule_type: Full-time
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
The Ecosystem Partner (EP) will deliver and differentiate the immunology value proposition to Executives and Population Stakeholders within influential Health Care Organizations (HCOs) - inclusive of Large Consolidated Groups (LCGs), Venture Capital/Private Equity (VC/PE), IDNs and Regional Payers. The EP will set strategic direction for targeted HCOs, develop, and foster strategic partnerships with Influencers to elevate UCB reputation, gather key insights and assist in achieving patient access to UCB products. The EP is responsible for identifying influencers, co-developing and implementing strategies in coordination with field partners, leveraging resources and internal expertise to develop productive and elevated relationships with key micro-ecosystem Executives and Population Health Stakeholders within influential HCOs. The goal is to establish a broad, deep, and coordinated network of relationships to elevate UCB’s reputation, align on initiatives to prioritize targeted patient populations, identify innovative partnerships, and achieve affordable product access for patients.
The Ecosystem Partner (EP) has primary responsibility to set the strategy at key influential HCOs and deliver and differentiate the Immunology value proposition raising awareness of prioritized patient populations to C-Suite and executive stakeholders within influential HCOs (per above).
You will contribute by:
• Demonstrating expertise and leadership with internal and external partners through an account management approach that leads to strategic partnerships that align with UCB priorities
• Modeling and leading strong squad and Immunology Patient Value Team collaboration and teamwork that contributes to achievement of shared objectives
• Coordinating with the market access partners, co-develop, define, and execute local strategic imperatives focused on maximizing UCB Immunology product access, affordability, and triage to the field partners for pull-through within the immunology micro-ecosystems
• Maintaining a keen understanding of immunology business including customers, brand marketing implementation strategies, business models, health economics, innovative population health initiatives, medical and pharmacy reimbursement, value-based care delivery models and bring insights back to the organization.
• Delivering and differentiating UCB with high impact, illuminating the immunology value proposition to Population Stakeholders across influential HCOs, and key immunology influencers in micro-ecosystems
• Delivering the differentiated immunology value proposition to key immunology formulary influencers in prioritized HCOs, developing advocates to optimize patient access, within regional payers/IDNs – across all immunology micro-ecosystems in coordination w market access partners
• Utilizing a deep understanding of influential HCOs within the ecosystem, inclusive of Regional Payer, IDN, VC/PE, ACO business models, functional infrastructure, and internal network connectivity, as well as key decision makers, immunology formulary influencers, and stakeholders aligned to the accounts.
• Being responsible for expanding broader and deeper relationships across diverse Immunology Clinical, Population Health, Utilization Management, Quality Teams, Innovation and Value-based care functions etc. – applied to multi-disciplinary formulary advocates internal to regional payers/IDNs – strategically coordinated with PVT and market access partners
• Operating at the highest level of UCB compliance and professional standards
Interested? For this position you’ll need the following education, experience and skills:
Minimum Requirements:
• Bachelors’ degree in life sciences, business or healthcare required
• 5-8 years of immunology and market access experience; sales leadership, marketing, or field medical experience preferred
• •3+ years in key account management
• Demonstrated experience and documented success leading multidisciplinary and/or matrixed teams
Preferred Requirements:
• Market expertise in US Immunology, Regional Payer/IDN, and Healthcare delivery systems preferred.
• Demonstrated leadership skills in managing, developing, and influencing teams.
• Demonstrated excellence in written and verbal communications
• Demonstrated strength in business planning, tactical plan development and execution.
• Masters’ degree in life sciences, business or healthcare required
About us.
At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.
With a team of approximately 7,600 employees and worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.
Curious to know more? Please visit our website www.ucb.com.
The Company is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, national origin, religion, gender, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.
Where permitted, applicants for employment in the United States must either have received or been willing to receive a full COVID-19 vaccination by the date of hire; or, alternatively, agree to be subject to weekly COVID-19 testing, subject to religious and medical exemptions and in accordance with applicable law Show more details...
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
The Ecosystem Partner (EP) will deliver and differentiate the immunology value proposition to Executives and Population Stakeholders within influential Health Care Organizations (HCOs) - inclusive of Large Consolidated Groups (LCGs), Venture Capital/Private Equity (VC/PE), IDNs and Regional Payers. The EP will set strategic direction for targeted HCOs, develop, and foster strategic partnerships with Influencers to elevate UCB reputation, gather key insights and assist in achieving patient access to UCB products. The EP is responsible for identifying influencers, co-developing and implementing strategies in coordination with field partners, leveraging resources and internal expertise to develop productive and elevated relationships with key micro-ecosystem Executives and Population Health Stakeholders within influential HCOs. The goal is to establish a broad, deep, and coordinated network of relationships to elevate UCB’s reputation, align on initiatives to prioritize targeted patient populations, identify innovative partnerships, and achieve affordable product access for patients.
The Ecosystem Partner (EP) has primary responsibility to set the strategy at key influential HCOs and deliver and differentiate the Immunology value proposition raising awareness of prioritized patient populations to C-Suite and executive stakeholders within influential HCOs (per above).
You will contribute by:
• Demonstrating expertise and leadership with internal and external partners through an account management approach that leads to strategic partnerships that align with UCB priorities
• Modeling and leading strong squad and Immunology Patient Value Team collaboration and teamwork that contributes to achievement of shared objectives
• Coordinating with the market access partners, co-develop, define, and execute local strategic imperatives focused on maximizing UCB Immunology product access, affordability, and triage to the field partners for pull-through within the immunology micro-ecosystems
• Maintaining a keen understanding of immunology business including customers, brand marketing implementation strategies, business models, health economics, innovative population health initiatives, medical and pharmacy reimbursement, value-based care delivery models and bring insights back to the organization.
• Delivering and differentiating UCB with high impact, illuminating the immunology value proposition to Population Stakeholders across influential HCOs, and key immunology influencers in micro-ecosystems
• Delivering the differentiated immunology value proposition to key immunology formulary influencers in prioritized HCOs, developing advocates to optimize patient access, within regional payers/IDNs – across all immunology micro-ecosystems in coordination w market access partners
• Utilizing a deep understanding of influential HCOs within the ecosystem, inclusive of Regional Payer, IDN, VC/PE, ACO business models, functional infrastructure, and internal network connectivity, as well as key decision makers, immunology formulary influencers, and stakeholders aligned to the accounts.
• Being responsible for expanding broader and deeper relationships across diverse Immunology Clinical, Population Health, Utilization Management, Quality Teams, Innovation and Value-based care functions etc. – applied to multi-disciplinary formulary advocates internal to regional payers/IDNs – strategically coordinated with PVT and market access partners
• Operating at the highest level of UCB compliance and professional standards
Interested? For this position you’ll need the following education, experience and skills:
Minimum Requirements:
• Bachelors’ degree in life sciences, business or healthcare required
• 5-8 years of immunology and market access experience; sales leadership, marketing, or field medical experience preferred
• •3+ years in key account management
• Demonstrated experience and documented success leading multidisciplinary and/or matrixed teams
Preferred Requirements:
• Market expertise in US Immunology, Regional Payer/IDN, and Healthcare delivery systems preferred.
• Demonstrated leadership skills in managing, developing, and influencing teams.
• Demonstrated excellence in written and verbal communications
• Demonstrated strength in business planning, tactical plan development and execution.
• Masters’ degree in life sciences, business or healthcare required
About us.
At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.
With a team of approximately 7,600 employees and worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.
Curious to know more? Please visit our website www.ucb.com.
The Company is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, national origin, religion, gender, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.
Where permitted, applicants for employment in the United States must either have received or been willing to receive a full COVID-19 vaccination by the date of hire; or, alternatively, agree to be subject to weekly COVID-19 testing, subject to religious and medical exemptions and in accordance with applicable law Show more details...
via UCB Careers
schedule_type: Full-time
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Quality Auditing and Compliance team, we are looking for a high caliber, self-motivated, Global Quality Auditing and Compliance Lead based in Atlanta, GA or Remote in the U.S..
At UCB everything we do starts with a simple question: “How will this make a difference to the lives of people living with severe diseases?” We do that by connecting our ground-breaking science with patients and their families around the world living with the physical and social burdens of autoimmune and neurological disorders. Those connections offer new perspectives, drive innovation, and offer the hope of a new generation of therapies that will help improve lives on a global scale.
You like to work in an environment where you will be able to:
• Lead and/or participate in the development of the risk based GCP audit program through evaluation of elements of the UCB quality system and their effect on the overall state of compliance of the system.
• Perform GCP audits as per annual audit program (investigator sites, vendors, systems, according to established audit strategy).
• Prepare, support and follow-up on GCP audits performed on behalf of UCB by external vendors and/or consultant auditors; as per established process, contracts and procedures. Ensure that execution of outsourced audits is conducted and completed in alignment with UCB audit processes and standards.
• Proactively manage findings, responses and CAPAs arising from audits in the Audit Management Tool, using all reasonable efforts to obtain prompt mitigation of deficiencies by responsible functions/persons and escalating concerns as required to senior management.
• As required, issue KPIs and dashboards that allow proper identification, follow-up and review of trends; providing a comprehensive summary and analyses of the comparative risks and outcomes across the GCP quality system.
• Contribute data and feedback to GCP-relevant internal stakeholders in UCB (e.g. Global Clinical Science and Operations, Global Clinical Development, Development Rare Disease, etc.) relating to Key Quality/Performance Indicators and quality compliance status.
• Support the preparation, hosting and follow up of Regulatory Authority inspections related to clinical activities, in collaboration with the Early and Dev Solutions Quality Management team.
• Through active participation to several forums and through direct interaction with colleagues, escalate concerns and provide expert guidance on GCP compliance issues to support the development and implementation of necessary CAPAS and quality improvement measures.
• Utilize in-depth knowledge and understanding of current business trends, applicable regulations and quality principles, to collaborate effectively and influence approaches to quality, and ensure work products and output are aligned with regulatory guidelines, ICH-GCP, other applicable regulatory requirements and UCB global quality standards.
• Participate in medium-long term projects within competence.
• Lead improvement initiatives, and where relevant, create and own the support in UCB Policies and standards, oversee their deployment including training material.
Interested? For this position you’ll need the following education, experience and skills:
• 5-10 years of background, knowledge and experience of the (bio)Pharma industry and applicable technical aspects of the business.
• Minimum of 5 years’ experience performing GCP related audits.
• Substantial and broad-ranging experience in the pharmaceutical/biotechnology area including significant time working in GCP-related areas.
• Experience with any of the following in clinical trials is advantageous: Decentralized and/or Hybrid Trials, Wearables, Digital Diagnostics, and/or Digital Biomarkers.
• Experience with application of regulatory requirements associated with the qualification, validation, implementation, use and life-cycle management of digital systems, tools and applications.
• Experience in leading full range of GCP audits for internal processes/units and external partners or vendors, and in managing/hosting regulatory inspections or third-party audits with depth of understanding of the theory and practice of quality.
Why you should apply
We can offer you an informal and open working environment that does not lock scientists into structure and hierarchy. Freedom to take space to pursue your own ideas and make a difference. Opportunity to gain internal and external visibility through interactions with other UCB teams and with world-renown academic investigators. Opportunity to grow both as a drug hunter and leader through participation in project teams and our career/personal development programs.
At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.
If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Quality Auditing and Compliance team, we are looking for a high caliber, self-motivated, Global Quality Auditing and Compliance Lead based in Atlanta, GA or Remote in the U.S..
At UCB everything we do starts with a simple question: “How will this make a difference to the lives of people living with severe diseases?” We do that by connecting our ground-breaking science with patients and their families around the world living with the physical and social burdens of autoimmune and neurological disorders. Those connections offer new perspectives, drive innovation, and offer the hope of a new generation of therapies that will help improve lives on a global scale.
You like to work in an environment where you will be able to:
• Lead and/or participate in the development of the risk based GCP audit program through evaluation of elements of the UCB quality system and their effect on the overall state of compliance of the system.
• Perform GCP audits as per annual audit program (investigator sites, vendors, systems, according to established audit strategy).
• Prepare, support and follow-up on GCP audits performed on behalf of UCB by external vendors and/or consultant auditors; as per established process, contracts and procedures. Ensure that execution of outsourced audits is conducted and completed in alignment with UCB audit processes and standards.
• Proactively manage findings, responses and CAPAs arising from audits in the Audit Management Tool, using all reasonable efforts to obtain prompt mitigation of deficiencies by responsible functions/persons and escalating concerns as required to senior management.
• As required, issue KPIs and dashboards that allow proper identification, follow-up and review of trends; providing a comprehensive summary and analyses of the comparative risks and outcomes across the GCP quality system.
• Contribute data and feedback to GCP-relevant internal stakeholders in UCB (e.g. Global Clinical Science and Operations, Global Clinical Development, Development Rare Disease, etc.) relating to Key Quality/Performance Indicators and quality compliance status.
• Support the preparation, hosting and follow up of Regulatory Authority inspections related to clinical activities, in collaboration with the Early and Dev Solutions Quality Management team.
• Through active participation to several forums and through direct interaction with colleagues, escalate concerns and provide expert guidance on GCP compliance issues to support the development and implementation of necessary CAPAS and quality improvement measures.
• Utilize in-depth knowledge and understanding of current business trends, applicable regulations and quality principles, to collaborate effectively and influence approaches to quality, and ensure work products and output are aligned with regulatory guidelines, ICH-GCP, other applicable regulatory requirements and UCB global quality standards.
• Participate in medium-long term projects within competence.
• Lead improvement initiatives, and where relevant, create and own the support in UCB Policies and standards, oversee their deployment including training material.
Interested? For this position you’ll need the following education, experience and skills:
• 5-10 years of background, knowledge and experience of the (bio)Pharma industry and applicable technical aspects of the business.
• Minimum of 5 years’ experience performing GCP related audits.
• Substantial and broad-ranging experience in the pharmaceutical/biotechnology area including significant time working in GCP-related areas.
• Experience with any of the following in clinical trials is advantageous: Decentralized and/or Hybrid Trials, Wearables, Digital Diagnostics, and/or Digital Biomarkers.
• Experience with application of regulatory requirements associated with the qualification, validation, implementation, use and life-cycle management of digital systems, tools and applications.
• Experience in leading full range of GCP audits for internal processes/units and external partners or vendors, and in managing/hosting regulatory inspections or third-party audits with depth of understanding of the theory and practice of quality.
Why you should apply
We can offer you an informal and open working environment that does not lock scientists into structure and hierarchy. Freedom to take space to pursue your own ideas and make a difference. Opportunity to gain internal and external visibility through interactions with other UCB teams and with world-renown academic investigators. Opportunity to grow both as a drug hunter and leader through participation in project teams and our career/personal development programs.
At UCB, we strive to attract passionate and outstanding talents who thrive on change and are ready to bring real value to patients. Working for us you’ll discover a place where you can grow and express your full potential. We place an emphasis on innovation, collaboration and impact. Through meaningful recognition and a motivating work atmosphere, we aim to provide an optimal experience by caring about and valuing our employees – just as we do for the patients we serve.
If you believe you are the perfect match to join us on our pioneering adventure, then we invite you to apply and tell us more about your profile and motivation.
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
via UCB Careers
schedule_type: Full-time
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Information Technology G2M team based in Smyrna, GA we are looking for a talented individual to fill the position of: Software Integration Engineer
As Software Integration Engineer, you will be driving IT initiatives requiring a very close collaboration with Transversal IT team, commercial data scientists, analysts, vendor partners and a good understanding/knowledge of the Azure tech stacks, Databricks, Snowflake, APIs, Integration environment and the challenges. You will lead the ideation and introduction of novel applications and software tools needed for the organization. The responsibility involves enabling Commercial stakeholders with cutting edge IT technologies by provisioning the use of Azure, Open source (AI/ML) software tools for the Commercial Analytics process.
You like to work in an environment where you can:
• Drive and lead software development projects and operations through ideation and manage day to-day business operations through novel applications and tools.
• Bring and introduce awareness of cutting-edge technologies among the internal commercial and IT community.
• Identify and enable technology & opportunities for continuous improvement to cover the unmet needs for G2M Solutions.
• Collaborate with application developers and operations based across the globe, coordinate and ensure the technology value delivery of projects, and the development team.
You will contribute by:
• Playing a crucial role as technology expert for the design and integration of the solutions.
• Interfacing with business stakeholders and IT teams (Architecture, Infrastructure, Security, and other groups at IT).
• Leading the technical design, development, integration, implementation, and support of key projects and operations
• Having expertise in technologies such as Data Pipeline build, data visualization, data integration, analytics in commercial environment.
• Easily managing the change by adopting to the pragmatic solutions and can handle the complex business problems, with can-do attitude.
For this position you'll need the following education, experience and skills:
Minimum Qualifications:
• Bachelor’s Degree in science or engineering or technology with +3 years of experience
• Previous experience within an application development, integration and production support is essential
• Cloud experience with Azure SQL Database, Azure SQL Data Warehouse, Azure Data Lake, Azure Data Synapse Analytics, Azure Data Factory, Azure ADLS, Azure Databricks, Event Hub for Streaming data, Azure DevOps
Preferred Qualifications:
• Experience preferably within Life Sciences (Pharma, BioTech) or healthcare industry
• Skilled in working with multidisciplinary teams, e.g. data analyst, data scientists, IT infra, networking, security and DevOps
• Modelling / Integration / Data analysis skills using common Data Mining and Machine Learning tools based on Python, R, Julia, Spark SQL programming languages
• Hands-on experience in integration design, coding, managing backlogs delivery of IS projects
• Proficient in data analysis, specification standards, vocabulary and glossary management, model building and data curation
• Exposure to natural language processing and machine learning
• Experience managing the end-to-end delivery of complex and dynamic situational project
• Penchant to learn about new technology innovation and creativity in applying to business problems
• Experience with Agile/Iterative Software Development Lifecycle (SDLC)
ITATUCB
About us.
At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.
With a team of approximately 7,600 employees and worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.
Curious to know more? Please visit our website www.ucb.com.
The Company is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, national origin, religion, gender, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.
Where permitted, applicants for employment in the United States must either have received or been willing to receive a full COVID-19 vaccination by the date of hire; or, alternatively, agree to be subject to weekly COVID-19 testing, subject to religious and medical exemptions and in accordance with applicable law Show more details...
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen our Information Technology G2M team based in Smyrna, GA we are looking for a talented individual to fill the position of: Software Integration Engineer
As Software Integration Engineer, you will be driving IT initiatives requiring a very close collaboration with Transversal IT team, commercial data scientists, analysts, vendor partners and a good understanding/knowledge of the Azure tech stacks, Databricks, Snowflake, APIs, Integration environment and the challenges. You will lead the ideation and introduction of novel applications and software tools needed for the organization. The responsibility involves enabling Commercial stakeholders with cutting edge IT technologies by provisioning the use of Azure, Open source (AI/ML) software tools for the Commercial Analytics process.
You like to work in an environment where you can:
• Drive and lead software development projects and operations through ideation and manage day to-day business operations through novel applications and tools.
• Bring and introduce awareness of cutting-edge technologies among the internal commercial and IT community.
• Identify and enable technology & opportunities for continuous improvement to cover the unmet needs for G2M Solutions.
• Collaborate with application developers and operations based across the globe, coordinate and ensure the technology value delivery of projects, and the development team.
You will contribute by:
• Playing a crucial role as technology expert for the design and integration of the solutions.
• Interfacing with business stakeholders and IT teams (Architecture, Infrastructure, Security, and other groups at IT).
• Leading the technical design, development, integration, implementation, and support of key projects and operations
• Having expertise in technologies such as Data Pipeline build, data visualization, data integration, analytics in commercial environment.
• Easily managing the change by adopting to the pragmatic solutions and can handle the complex business problems, with can-do attitude.
For this position you'll need the following education, experience and skills:
Minimum Qualifications:
• Bachelor’s Degree in science or engineering or technology with +3 years of experience
• Previous experience within an application development, integration and production support is essential
• Cloud experience with Azure SQL Database, Azure SQL Data Warehouse, Azure Data Lake, Azure Data Synapse Analytics, Azure Data Factory, Azure ADLS, Azure Databricks, Event Hub for Streaming data, Azure DevOps
Preferred Qualifications:
• Experience preferably within Life Sciences (Pharma, BioTech) or healthcare industry
• Skilled in working with multidisciplinary teams, e.g. data analyst, data scientists, IT infra, networking, security and DevOps
• Modelling / Integration / Data analysis skills using common Data Mining and Machine Learning tools based on Python, R, Julia, Spark SQL programming languages
• Hands-on experience in integration design, coding, managing backlogs delivery of IS projects
• Proficient in data analysis, specification standards, vocabulary and glossary management, model building and data curation
• Exposure to natural language processing and machine learning
• Experience managing the end-to-end delivery of complex and dynamic situational project
• Penchant to learn about new technology innovation and creativity in applying to business problems
• Experience with Agile/Iterative Software Development Lifecycle (SDLC)
ITATUCB
About us.
At UCB, we come together every day to work, laser-focused, on a simple question: How will this create value for people living with severe diseases? By putting patients at the heart of everything we do, our approach – from discovery to development to delivery – is continuously transformed and designed around patient needs and their journey.
With a team of approximately 7,600 employees and worldwide operations in more than 40 countries, we are a global biopharmaceutical company investing more than a quarter of our revenue in cutting-edge scientific research. We are focused on addressing chronic, neurological, immunological, and bone diseases. We are looking for people with passion and empathy who develop a real understanding of patient’s needs and can deliver thoughtful solutions to decisionmakers across the heath care ecosystem.
Curious to know more? Please visit our website www.ucb.com.
The Company is an equal opportunity employer. We evaluate qualified applicants without regard to race, color, national origin, religion, gender, age, marital status, disability, veteran status, sexual orientation, gender identity, or any other characteristic protected by law.
Where permitted, applicants for employment in the United States must either have received or been willing to receive a full COVID-19 vaccination by the date of hire; or, alternatively, agree to be subject to weekly COVID-19 testing, subject to religious and medical exemptions and in accordance with applicable law Show more details...
via UCB Careers
posted_at: 3 days agoschedule_type: Full-time
Make your mark for patients
We are looking for a National Lead, Health Outcomes Value & Access (HOVA) to join us in our Health Economics & Outcomes Research (HEOR) strategy team based in the US. This is a remote, field based position...
About the role
This individual will lead both medical and HEOR engagements at national accounts including national health plans and PBMs, their subsidiaries and key strategic partners and stakeholders. The National
Make your mark for patients
We are looking for a National Lead, Health Outcomes Value & Access (HOVA) to join us in our Health Economics & Outcomes Research (HEOR) strategy team based in the US. This is a remote, field based position...
About the role
This individual will lead both medical and HEOR engagements at national accounts including national health plans and PBMs, their subsidiaries and key strategic partners and stakeholders. The National Lead, HOVA, will be responsible for developing and implementing account-specific HEOR and Medical strategies to enhance payers’ understanding of UCB’s value proposition in improving health outcomes for patients living with severe chronic diseases.
Who you’ll work with
This lead will play a key role in the support and execution of population health engagements with national payers, policymakers, and other relevant stakeholders to achieve optimal understanding of relevant HEOR data related to UCB products and disease state. This individual will work closely with access strategy leads to generate impactful insights and partner with respective cross-functional colleagues in to ensure alignment with HEOR, Medical, and access strategy.
What you’ll do
• Lead the development and execution of HEOR and Medical engagement strategies with National and key Regional Accounts
• Lead the development and execution of HEOR strategies with therapeutic area access strategy leads
• Lead strategic HEOR and Medical engagements with internal stakeholders to ensure alignment of therapeutic area HEOR plans with patient value and access needs
• Leverage HEOR methodologies and expertise in electronic medical records, administrative claims databases, and/or registries to support value-based contracting concepts
• Develop and manage customer engagement and relationships within targeted accounts. This includes identifying individuals involved in HEOR, outcomes, value assessments, RWE data generation, quality, IT, AI and other key functions relevant to HEOR
• Assess clinical and economic data gaps at key national accounts and collaborate with internal stakeholders to provide insight into HEOR needs
• Lead the creation of relevant HEOR resources to effectively engage external stakeholders
• Provide HEOR strategic support in innovation and partnership opportunities including RWE collaborations and value-based contracting efforts
• Establish, foster, and grow relationships with key decision-makers and influencers
Interested? For this role we’re looking for the following education, experience and skills
• MD, PharmD or PhD (in a related field)
• Ability to critically assess and analyze clinical and HEOR data gaps and provide relevant medical solutions
• Proven ability to grow and foster key relationships in payer accounts to enhance insights needed to align internal HEOR strategies for continued alignment with healthcare trends and success
• Minimum of 3+ years in the field engaging with US payers
• Established track record of effective oral presentation within healthcare settings including presentations to C-Suite executives across medical and commercial
• Strong understanding of the rapidly evolving healthcare landscape and demonstrated ability to generate actionable insight to enhance and execute internal HEOR strategies
• Strong understanding of cost-effectiveness modeling and HTA methods to engage in payer and policy discussions with proficiency and confidence
• Ability to travel, estimated travel is 25%
Preferred Qualifications:
• Completion of an HEOR Fellowship or relevant experience (i.e. education in public health, epidemiology, applied health economics)
• 5+ years prior experience in managed care, ideally with large regional or national accounts
• 5+ years pharmaceutical industry or relevant experience
• Industry experience in chronic inflammatory disease or neurology =
• Publications (abstracts, posters, manuscript) demonstrating proficiency in HEOR study design and execution
• Demonstrated success in HEOR partnerships (i.e. RWE collaborations)
Target compensation commensurate with experience, skills & location: $175,000-$225,000
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
Why work for us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
Learn more about sustainability at UCB and how it is integrated into our business approach.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
We are looking for a National Lead, Health Outcomes Value & Access (HOVA) to join us in our Health Economics & Outcomes Research (HEOR) strategy team based in the US. This is a remote, field based position...
About the role
This individual will lead both medical and HEOR engagements at national accounts including national health plans and PBMs, their subsidiaries and key strategic partners and stakeholders. The National Lead, HOVA, will be responsible for developing and implementing account-specific HEOR and Medical strategies to enhance payers’ understanding of UCB’s value proposition in improving health outcomes for patients living with severe chronic diseases.
Who you’ll work with
This lead will play a key role in the support and execution of population health engagements with national payers, policymakers, and other relevant stakeholders to achieve optimal understanding of relevant HEOR data related to UCB products and disease state. This individual will work closely with access strategy leads to generate impactful insights and partner with respective cross-functional colleagues in to ensure alignment with HEOR, Medical, and access strategy.
What you’ll do
• Lead the development and execution of HEOR and Medical engagement strategies with National and key Regional Accounts
• Lead the development and execution of HEOR strategies with therapeutic area access strategy leads
• Lead strategic HEOR and Medical engagements with internal stakeholders to ensure alignment of therapeutic area HEOR plans with patient value and access needs
• Leverage HEOR methodologies and expertise in electronic medical records, administrative claims databases, and/or registries to support value-based contracting concepts
• Develop and manage customer engagement and relationships within targeted accounts. This includes identifying individuals involved in HEOR, outcomes, value assessments, RWE data generation, quality, IT, AI and other key functions relevant to HEOR
• Assess clinical and economic data gaps at key national accounts and collaborate with internal stakeholders to provide insight into HEOR needs
• Lead the creation of relevant HEOR resources to effectively engage external stakeholders
• Provide HEOR strategic support in innovation and partnership opportunities including RWE collaborations and value-based contracting efforts
• Establish, foster, and grow relationships with key decision-makers and influencers
Interested? For this role we’re looking for the following education, experience and skills
• MD, PharmD or PhD (in a related field)
• Ability to critically assess and analyze clinical and HEOR data gaps and provide relevant medical solutions
• Proven ability to grow and foster key relationships in payer accounts to enhance insights needed to align internal HEOR strategies for continued alignment with healthcare trends and success
• Minimum of 3+ years in the field engaging with US payers
• Established track record of effective oral presentation within healthcare settings including presentations to C-Suite executives across medical and commercial
• Strong understanding of the rapidly evolving healthcare landscape and demonstrated ability to generate actionable insight to enhance and execute internal HEOR strategies
• Strong understanding of cost-effectiveness modeling and HTA methods to engage in payer and policy discussions with proficiency and confidence
• Ability to travel, estimated travel is 25%
Preferred Qualifications:
• Completion of an HEOR Fellowship or relevant experience (i.e. education in public health, epidemiology, applied health economics)
• 5+ years prior experience in managed care, ideally with large regional or national accounts
• 5+ years pharmaceutical industry or relevant experience
• Industry experience in chronic inflammatory disease or neurology =
• Publications (abstracts, posters, manuscript) demonstrating proficiency in HEOR study design and execution
• Demonstrated success in HEOR partnerships (i.e. RWE collaborations)
Target compensation commensurate with experience, skills & location: $175,000-$225,000
Are you ready to ‘go beyond’ to create value and make your mark for patients? If this sounds like you, then we would love to hear from you!
About us
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 8,500 people in all four corners of the globe, inspired by patients and driven by science.
Why work for us?
At UCB, we don’t just complete tasks, we create value. We aren’t afraid to push forward, collaborate, and innovate to make our mark for patients. We have a caring, supportive culture where everyone feels included, respected and has equitable opportunities to do their best work. We ‘go beyond’ to create value for our patients, and always with a human focus, whether that’s on our patients, our employees or our planet. Working for us, you will discover a place where you can grow, and have the freedom to carve your own career path to achieve your full potential.
Learn more about sustainability at UCB and how it is integrated into our business approach.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer. We do not discriminate on the basis of race/colour/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity Show more details...
via ASGCT Career Center
posted_at: 11 days agoschedule_type: Full-time
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of
Make your mark for patients.
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen theQuantitative Clinical PharmacologyGroup, based at our research site in Slough, we are seeking a talented individual to fill the position ofQuantitative Clinical Pharmacology Lead.
You like to work in an environment where you can:
Demonstrate experience in strategically leading clinical pharmacology input for large or small molecules into development programs from pre-FIH to life-cycle management.
You will contribute by:
Leading and scoping the quantitative clinical pharmacology activities in assigned project(s) to drive further Early and Late Clinical Development within UCB, working with other functional experts to create a clinical development plan.
In collaboration with other disciplines, he/she will be accountable and responsible for leading and driving, for the assigned project(s), an integrated PK-PD strategy (safety and efficacy) from clinical candidate selection through life-cycle management, driving dose and regimen selection and drive the implementation of model informed drug development, including trial design and execution.
As a key member of quantitative discovery and development (QDD) and development sciences, you will foster and facilitate a collaborative working environment between non-clinical safety, DMPK, bioanalysis, non-clinical PK-PD, modelling and simulation to leverage key scientific and strategic input into projects.
From a development science perspective, you may also be responsible to ensure a clear development science strategy is formed and lead a matrix team covering; QCP, Modelling and Simulation, DMPK, Toxicology and Bioanalytical ensuring clear deliverables and key milestones are achieved and drive project decisions. He/she will also ensure high quality and robust input is given into development teams.
Interested? For this position you’ll need the following education, experience and skills:
Educated to PharmD or PhD (or equivalent) with either relevant academic or industrial experience.
You will have demonstrated experience (through examples) of participating and contributing to the development and execution of the clinical plan, with specific input and expertise in the clinical pharmacology components, including regulatory aspects (e.g briefing documents, MHRA meetings, pediatric plans, INDs, regulatory responses for labelling activities), and is able to attend regulatory meetings representing function and UCB with minimal coaching.
A strong understanding of pharmacodynamic and translational methods, experimental medicine tools, regulatory requirements, PK/PD, DMPK, population pharmacokinetic-pharmacodynamic modelling and simulation.
RANDATUCB
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer.We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.
Demonstrate experience in strategically leading clinical pharmacology input for large or small molecules into development programs from pre-FIH to life-cycle management. Leading and scoping the quantitative clinical pharmacology activities in assigned project(s) to drive further Early and Late Clinical Development within UCB, working with other functional experts to create a clinical development plan. In collaboration with other disciplines, he/she will be accountable and responsible for leading and driving, for the assigned project(s), an integrated PK-PD strategy (safety and efficacy) from clinical candidate selection through life-cycle management, driving dose and regimen selection and drive the implementation of model informed drug development, including trial design and execution. As a key member of quantitative discovery and development (QDD) and development sciences, you will foster and facilitate a collaborative working environment between non-clinical safety, DMPK, bioanalysis, non-clinical PK-PD, modelling and simulation to leverage key scientific and strategic input into projects. From a development science perspective, you may also be responsible to ensure a clear development science strategy is formed and lead a matrix team covering; QCP, Modelling and Simulation, DMPK, Toxicology and Bioanalytical ensuring clear deliverables and key milestones are achieved and drive project decisions. He/she will also ensure high quality and robust input is given into development teams. You will have demonstrated experience (through examples) of participating and contributing to the development and execution of the clinical plan, with specific input and expertise in the clinical pharmacology components, including regulatory aspects (e.g briefing documents, MHRA meetings, pediatric plans, INDs, regulatory responses for labelling activities), and is able to attend regulatory meetings representing function and UCB with minimal coaching. Make your mark for patients. Development, Clinical Pharmacology, Clinical, Pharmacodynamic, Pharmacokinetic, Science, Clinical Development, Bioanalysis, Toxicology, Small Molecules, Clinical Safety, Regulatory, Safety, Milestones, Regulatory Requirements, Management, dmpk, Simulation, pk-pd strategy, Industrial Experience, Coaching, Collaborative Working, Candidate Selection, Senior Scientist, Principal Scientist, Principal Research Scientist, Senior Research Scientist, Associate Scientist, Marketing Manager - Process Chromatography, Research Associate - Biology II, DevOps Research & Development, Senior Statistician, Research & Development Co-Op Show more details...
We’re here because we want to build the future and transform patients’ lives for the better...
At UCB, our people are our experiences and achievements, our passion and drive. That’s why we’re looking for talented individuals with diverse backgrounds and experiences - not just the best and brightest, but those who care about making a meaningful difference in the lives of patients. We promote an environment of diversity, openness, and respect where people can make valuable contributions.
An exciting journey lies ahead. Will you join us in pushing the boundaries of what’s possible?
To strengthen theQuantitative Clinical PharmacologyGroup, based at our research site in Slough, we are seeking a talented individual to fill the position ofQuantitative Clinical Pharmacology Lead.
You like to work in an environment where you can:
Demonstrate experience in strategically leading clinical pharmacology input for large or small molecules into development programs from pre-FIH to life-cycle management.
You will contribute by:
Leading and scoping the quantitative clinical pharmacology activities in assigned project(s) to drive further Early and Late Clinical Development within UCB, working with other functional experts to create a clinical development plan.
In collaboration with other disciplines, he/she will be accountable and responsible for leading and driving, for the assigned project(s), an integrated PK-PD strategy (safety and efficacy) from clinical candidate selection through life-cycle management, driving dose and regimen selection and drive the implementation of model informed drug development, including trial design and execution.
As a key member of quantitative discovery and development (QDD) and development sciences, you will foster and facilitate a collaborative working environment between non-clinical safety, DMPK, bioanalysis, non-clinical PK-PD, modelling and simulation to leverage key scientific and strategic input into projects.
From a development science perspective, you may also be responsible to ensure a clear development science strategy is formed and lead a matrix team covering; QCP, Modelling and Simulation, DMPK, Toxicology and Bioanalytical ensuring clear deliverables and key milestones are achieved and drive project decisions. He/she will also ensure high quality and robust input is given into development teams.
Interested? For this position you’ll need the following education, experience and skills:
Educated to PharmD or PhD (or equivalent) with either relevant academic or industrial experience.
You will have demonstrated experience (through examples) of participating and contributing to the development and execution of the clinical plan, with specific input and expertise in the clinical pharmacology components, including regulatory aspects (e.g briefing documents, MHRA meetings, pediatric plans, INDs, regulatory responses for labelling activities), and is able to attend regulatory meetings representing function and UCB with minimal coaching.
A strong understanding of pharmacodynamic and translational methods, experimental medicine tools, regulatory requirements, PK/PD, DMPK, population pharmacokinetic-pharmacodynamic modelling and simulation.
RANDATUCB
About us.
UCB is a global biopharmaceutical company, focusing on neurology and immunology. We are around 7,600 people in all four corners of the globe, inspired by patients and driven by science.
At UCB, everything we do start with a simple question: “How will this create value for people living with severe disease?”. We are on a journey to become the patient-preferred biopharma leader by delivering medicines and solutions that improve lives. We want to ensure the creation of patient value, now and into the future, while contributing to a society where a population of 8 billion people and more should be able to live a good life within limited resources of one planet.
Curious to know more? Please visit our website www.ucb.com.
UCB and its subsidiaries encourage diversity and inclusion in the workplace; we are an Equal Opportunity Employer.We do not discriminate on the basis of race/color/religion/sex/national origin/veteran/disability/age/sexual orientation/gender identity.
Demonstrate experience in strategically leading clinical pharmacology input for large or small molecules into development programs from pre-FIH to life-cycle management. Leading and scoping the quantitative clinical pharmacology activities in assigned project(s) to drive further Early and Late Clinical Development within UCB, working with other functional experts to create a clinical development plan. In collaboration with other disciplines, he/she will be accountable and responsible for leading and driving, for the assigned project(s), an integrated PK-PD strategy (safety and efficacy) from clinical candidate selection through life-cycle management, driving dose and regimen selection and drive the implementation of model informed drug development, including trial design and execution. As a key member of quantitative discovery and development (QDD) and development sciences, you will foster and facilitate a collaborative working environment between non-clinical safety, DMPK, bioanalysis, non-clinical PK-PD, modelling and simulation to leverage key scientific and strategic input into projects. From a development science perspective, you may also be responsible to ensure a clear development science strategy is formed and lead a matrix team covering; QCP, Modelling and Simulation, DMPK, Toxicology and Bioanalytical ensuring clear deliverables and key milestones are achieved and drive project decisions. He/she will also ensure high quality and robust input is given into development teams. You will have demonstrated experience (through examples) of participating and contributing to the development and execution of the clinical plan, with specific input and expertise in the clinical pharmacology components, including regulatory aspects (e.g briefing documents, MHRA meetings, pediatric plans, INDs, regulatory responses for labelling activities), and is able to attend regulatory meetings representing function and UCB with minimal coaching. Make your mark for patients. Development, Clinical Pharmacology, Clinical, Pharmacodynamic, Pharmacokinetic, Science, Clinical Development, Bioanalysis, Toxicology, Small Molecules, Clinical Safety, Regulatory, Safety, Milestones, Regulatory Requirements, Management, dmpk, Simulation, pk-pd strategy, Industrial Experience, Coaching, Collaborative Working, Candidate Selection, Senior Scientist, Principal Scientist, Principal Research Scientist, Senior Research Scientist, Associate Scientist, Marketing Manager - Process Chromatography, Research Associate - Biology II, DevOps Research & Development, Senior Statistician, Research & Development Co-Op Show more details...
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