cambridgeusa

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  • Country
    Hosted in United States

  • Traffic rank
    #814,232 Site Rank

  • Site age
    13 yrs old

  • Site Owner information
    Whois info

Traffic rank
#814,232
Site age
13 yrs
Location
United States
Newest job postings for cambridgeusa
via Adecco Staffing posted_at: 4 days agoschedule_type: Full-time
decco Medical & Science is seeking a Scientist I for a seven-month contract with our Pharmaceutical partner in Cambridge, MA The anticipated wage for this position is between $54 and $55.40. Hourly wage may depend upon experience, education, geographic location, and other factors... Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. decco Medical & Science is seeking a Scientist I for a seven-month contract with our Pharmaceutical partner in Cambridge, MA

The anticipated wage for this position is between $54 and $55.40. Hourly wage may depend upon experience, education, geographic location, and other factors...

Benefit offerings include medical, dental, vision, life insurance, short-term disability, additional voluntary benefits, EAP program, commuter benefits and 401K plan. Our program provides employees the flexibility to choose the type of coverage that meets their individual needs. Available paid leave may include Paid Sick Leave, where required by law; any other paid leave required by Federal, State, or local law; and Holiday pay upon meeting eligibility criteria.

Job Description:
The Autoimmunity & Type 1 Diabetes Cluster, within the Immunology & Inflammation Therapeutic Area (TA), aims to discover new mechanistic pathways in autoimmune diseases and develop these findings into novel disease-modifying drugs that improve the lives of patients. Our focus is on inflammatory diseases driven by self-reactivity and characterized by loss of immunological tolerance. The current major emphasis is on systemic lupus erythematosus and type 1 diabetes but may extend into other immune-mediated areas (such as multiple sclerosis, rheumatological and antibody-mediated diseases) when our science and discoveries lead us.
We wish to recruit a Senior Associate Scientist who will work in a dynamic, matrix laboratory team environment, with the aim of identifying new disease targets and taking these through to drug development. Our target discovery process is facilitated by extensive collaboration across our other TA Clusters (focused on Checkpoint Immunity, Type 2 Inflammation & Fibrosis, Type 1 and Type 17 Immunity, and Precision Immunology) as well as with our platforms in drug discovery, biologic molecules, and disease model pharmacology.
The successful candidate should have a solid background in immunology and demonstrated ability to integrate into projects/assignments as part of a dynamic team, contributing technical skills and functional knowledge. Evidence of technical expertise in APC and T/B-cell biology, immune regulation, immune tolerance, and cytokine biology is highly desirable, as well as experience developing novel immunoassays and finding solutions to technical or research questions. S/he should be able to work with a high degree of flexibility and under limited supervision, managing time efficiently to enable contribution to multiple projects simultaneously. The candidate will join a Cluster that is committed to finding solutions to autoimmune diseases and comprises three other laboratory teams, each with senior scientific leadership and similar goals.

Job Responsibilities:
• Participate in programs through design and execution of laboratory experiments to identify novel targets and develop therapeutic molecules to modulate pathways for autoimmune disease intervention.
• Coordinate studies with group members as well as with our colleagues in other TA Clusters and platforms such as in vivo pharmacology.
• Oral and written communication of projects and data packages to varied audiences.
• Maintain awareness of current scientific developments in our field and integrate this knowledge into our activities.
• Mentor scientists in the Cluster and be accountable for effective performance of the team and its individuals.
• Ensure productive and efficient utilization of department resources to meet project timelines.
• Understand and adhere to corporate standards regarding code of conduct, safety, and appropriate handling and disposal of materials such as controlled drug substances, biohazardous material, and radioactive compounds.

Qualifications:
Basic qualifications and requirements include:
• Bachelors Degree plus a minimum of 4 years OR Masters Degree plus a minimum of 1 year of relevant research experience in an academic or biopharmaceutical setting; hands-on industry experience designing, executing, and documenting of compound validation and testing experiments
• Demonstrated background in cellular immunology is essential: experience isolating primary mouse and human immune cell subsets for utilization in immunological assays would be highly desirable as would working knowledge of multi-color flow cytometry and FACS-based immunophenotyping; in vivo mouse experience (live handling, post-mortem tissue acquisition), or the willingness to learn, would be highly desirable but not required.
• Proficiency across cellular, biochemical, and molecular techniques, which may include: stable cell line generation and characterization, protein detection (ELISA, MSD, Luminex), and gene profiling (RT-PCR, NanoString, NGS).
• S/he must be scientifically rigorous, highly organized, and self-motivated; must be able to work independently while interacting and maintaining strong working relationships with a diverse group of research collaborators.
• Demonstrated curiosity and ability to master new scientific disciplines, troubleshoot both technical and scientific problems, and analyze and interpret experimental data and suggest next steps.
• Ability to effectively present and communicate complex data sets to diverse audiences.
Years of Experience: 0 - 3 Years

Equal Opportunity Employer/Veterans/Disabled

To read our Candidate Privacy Information Statement, which explains how we will use your information, please navigate to https://www.adeccousa.com/candidate-privacy

The Company will consider qualified applicants with arrest and conviction records
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via Google Careers posted_at: 19 days agoschedule_type: Full-time
The Private Advertising Technology team is working on using cutting edge confidential computing technologies to evolve the APIs and infrastructure in Chrome and Android that support advertising use cases while limiting user tracking. The Platforms and Ecosystems product area encompasses Google's various computing software platforms across environments (desktop, mobile, applications). The... products provide enterprises, and ultimately end users, The Private Advertising Technology team is working on using cutting edge confidential computing technologies to evolve the APIs and infrastructure in Chrome and Android that support advertising use cases while limiting user tracking.

The Platforms and Ecosystems product area encompasses Google's various computing software platforms across environments (desktop, mobile, applications). The... products provide enterprises, and ultimately end users, the ability to utilize and manage their services at scale. We build innovative and compelling software products—from apps to TVs, from laptops to phones—that have an impact on people’s lives across the world.

The US base salary range for this full-time position is $185,000-$283,000 + bonus + equity + benefits. Our salary ranges are determined by role, level, and location. The range displayed on each job posting reflects the minimum and maximum target for new hire salaries for the position across all US locations. Within the range, individual pay is determined by work location and additional factors, including job-related skills, experience, and relevant education or training. Your recruiter can share more about the specific salary range for your preferred location during the hiring process.

Please note that the compensation details listed in US role postings reflect the base salary only, and do not include bonus, equity, or benefits. Learn more about benefits at Google
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via Nexxt posted_at: 3 days agoschedule_type: Contractor
usa - medical director. • cambridge , massachusetts • posted may 18, 2023... job details summary • $110 - $117.82 per hour • contract • postgraduate degree • category life, physical, and social science occupations • reference45681 job details job summary: As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences usa - medical director.
• cambridge , massachusetts
• posted may 18, 2023...

job details

summary
• $110 - $117.82 per hour
• contract
• postgraduate degree
• category life, physical, and social science occupations
• reference45681

job details

job summary:

As the largest staffing and recruitment agency in the world, we can commit to finding you the perfect role that gives you the opportunity to learn and grow in the life sciences arena. Utilizing a recruiter for your job search gives you access to a large network of top employers as well as detailed information about hundreds of positions. Our partner recognizes the need for innovative care and utilizes Research & Development to further knowledge in Oncology, Neuroscience, Rare Diseases, and Gastroenterology. As a company that brings in over $30 billion in annual revenue, they have established themselves as a biopharmaceutical powerhouse that is changing the world. If you're looking for a position where your work will benefit millions of people, we are waiting for you!

location: Cambridge, Massachusetts

job type: Contract

salary: $110.00 - 117.82 per hour

work hours: 9 to 5

education: Doctorate

responsibilities:
• Lead Clinical Development for a given product and/or indication, and may represent Clinical Medicine on the Global (US/EU/Japan) Clinical Development Team to ensure that activities are aligned with the global strategy
• Establishes and drives development team strategy and deliverables producing the development strategy, Clinical Development Plan and Clinical Protocols
• Responsible for high impact global decisions: monitoring and interpreting data from ongoing internal and external studies, assessing the medical and scientific implications and making recommendations that impact regional and global development such as "go/no go" decisions or modification of development plans or study designs that may have a significant impact on timelines or product labeling

qualifications:

Requirements:
• M.D. or internationally recognized equivalent degree
• 5 years of strong clinical research/drug development experience in the pharmaceutical industry
• Previous experience leading a clinical development team/matrix team with responsibility for studies in multiple regions. Development experience beyond US/EU
• Experience in patient care or academia is required
• Clinical or research background in Neurology, Neuroscience, Immunology or related specialties relevant to disease mechanisms and plasma derived/related therapies
• Scientific writing experience (eg: reflected by publications, grant submissions)

skills: Clinical research, MS-WORD, MS-EXCEL, MS-Powerpoint

Equal Opportunity Employer: Race, Color, Religion, Sex, Sexual Orientation, Gender Identity, National Origin, Age, Genetic Information, Disability, Protected Veteran Status, or any other legally protected group status.

At Randstad, we welcome people of all abilities and want to ensure that our hiring and interview process meets the needs of all applicants. If you require a reasonable accommodation to make your application or interview experience a great one, please contact ~~~.

Pay offered to a successful candidate will be based on several factors including the candidate's education, work experience, work location, specific job duties, certifications, etc. In addition, Randstad offers a comprehensive benefits package, including health, an incentive and recognition program, and 401K contribution (all benefits are based on eligibility).

For certain assignments, Covid-19 vaccination and/or testing may be required by Randstad's client or applicable federal mandate, subject to approved medical or religious accommodations. Carefully review the job posting for details on vaccine/testing requirements or ask your Randstad representative for more information
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