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Forma Therapeutics Holdings, Inc
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Watertown, MA
Forma is seeking a talented and highly motivated Lead or Senior Clinical Data Manager, who will serve as the Sponsor Data Manager on a portfolio of Phase I-III clinical trials....
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2 days ago
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IT ELITE INC
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Northbrook, IL
Strong knowledge of medical terminology and the clinical trial process is required. Experience with Clinical Database experience as well as SAS dataset structure....
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1 day ago
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Cambridge, MA
Manage clinical trial data through review, cleaning, auditing, validation procedures and ensure data handling compliance with regulatory requirements, especially as it pertains to electronic Diary data...
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20 hours ago
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Irvine, PA
S/he ensures clinical trial data collected meet the highest standards of data integrity, while meeting timelines and budgets....
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18 hours ago
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23andMe, Inc.
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South San Francisco, CA
In-depth understanding of cross-functional team roles and responsibilities involved in drug development....
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2 days ago
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Planet Pharma
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Remote, OR
Knowledgeable about the critical elements for success in clinical trials; participation in and contribution to these activities....
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2 days ago
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Brisbane, CA
collection activities satisfy the clinical trial regulation and requirements Assist in generating datasets for analysis and reporting by supporting the cross-functional team of different stakeholders...
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19 hours ago
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CAMRIS International
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Bethesda, MD
Must have experience with ICH/GCP...
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2 days ago
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Planet Pharma
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Culver City, CA
Recommended skills Attention To Detail Team Working Self Motivation Curiosity Success Driven Clinical Trials...
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3 days ago
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Becton, Dickinson and Company
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Franklin Lakes, NJ
Job Description Essential Job Functions: Review study protocols to ensure the data collection requirements are clear and supportive of the study endpoints....
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3 days ago
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Xencor, Inc.
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San Diego, CA
trial Requirements: Strong knowledge of drug development processes Proven success in management of CDM, projects, vendors, CRO's Excellent management, collaboration, communication, and decision-making...
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4 days ago
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System One
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Irvine, CA
S/he ensures clinical trial data collected meet the highest standards of data integrity, while meeting timelines and budgets....
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4 days ago
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Meridian Health System
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Hackensack, NJ
Reports, tracks, and files off-site Serious Adverse Events (SAEs) to the governing Institutional Review Board (IRB) within the required time frame dictated by the IRB of record....
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4 days ago
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Deciphera Pharmaceuticals, LLC
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Waltham, MA
development....
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5 days ago
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Loxo Oncology, Inc.
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Boulder, CO
, GCP, PhRMA, Privacy, etc) to data collection and DM plans Collaborate and oversee CRO/service providers on assigned studies Executes/manages all data management activities on assigned studies to ensure...
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5 days ago
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