• Technical Investigator

    Meta (Trenton, NJ)
    …outcomes, and scale solutions to protect Meta users from harm. **Required Skills:** Technical Investigator , Integrity Operations Responsibilities: 1. ... **Summary:** The Behavior Integrity Operations team within Integrity...Products at scale. In this role, you will conduct technical network investigations to identify, mitigate, and prevent bad… more
    Meta (04/18/25)
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  • Director, Clinical Pharmacology Lead

    Organon & Co. (Jersey City, NJ)
    …2a study protocols, in collaboration with internal (biostatistics, clinical operations ) and external (contract research organization [CRO], bioanalytical and/or ... study director responsible for the execution (in conjunction with the TMED Operations Lead) and reporting thereof. The Director will work collaboratively with… more
    Organon & Co. (04/29/25)
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  • aT1D Medical Program Lead

    Sanofi Group (Morristown, NJ)
    …Job** Under the oversight of the US General Medicines Program Optimization & Operations Lead, the autoimmune Type 1 Diabetes Medical Program Lead (aT1D MPL) will, ... (eg, local concept/protocol review) and all subsequent applicable aspects of Investigator Sponsored Studies (ISSs) and Externally Sponsored Collaborations (ESCs) to… more
    Sanofi Group (04/04/25)
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  • Clinical Trial Manager

    Actalent (Princeton, NJ)
    …to time, budget, and quality objectives. + Implement globally agreed Development Operations strategies, including processes and technical systems related to ... Trial ManagerJob Description The Clinical Trial Manager acts as a vital operations leader within the global study team, ensuring quality, consistency, and… more
    Actalent (05/21/25)
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  • Clinical Lead, I&I

    Sanofi Group (Morristown, NJ)
    …opportunities as needed + Apply high ethical standards and work with integrity **About You** **Scientific and technical Expertise:** This position requires ... endorsement by governance and its execution in close collaboration with clinical operations . The clinical lead is expected to advance scientific and clinical… more
    Sanofi Group (05/01/25)
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  • Clinical Research Director

    Sanofi Group (Morristown, NJ)
    …development opportunities as needed. + apply high ethical standards and work with integrity . **Scientific and Technical Expertise:** + This position requires a ... its endorsement by governance and its execution in close collaboration with clinical operations . The CRD is expected to advance scientific and clinical knowledge for… more
    Sanofi Group (04/06/25)
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  • Medical Director or Scientific Director, Medical…

    AbbVie (Florham Park, NJ)
    …analysis, interpretation, and reporting of scientific content of protocols, Investigator Brochures, Clinical Study Reports and regulatory submissions and responses. ... of the Medical Affairs-led clinical studies, monitoring overall study integrity and review, interpretation and communication of accumulating data pertaining… more
    AbbVie (05/10/25)
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  • Senior Clinical Scientist, Immunology

    Bristol Myers Squibb (Princeton, NJ)
    …of site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (eg, DMC) activities + Drafting/review ... knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations + Proficient knowledge and skills to support program specific data… more
    Bristol Myers Squibb (05/21/25)
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  • Manager, Data Management

    Daiichi Sankyo Inc. (Basking Ridge, NJ)
    …management processes, Electronic Data Capture (EDC)/related applications, industry standards, and technical skills in working with data received from CROs and other ... and cultures. Additionally, this position requires knowledge of clinical operations , biostatistics, and relevant regulatory requirements. This position requires… more
    Daiichi Sankyo Inc. (05/15/25)
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  • Senior Clinical Scientist, Early Development…

    Bristol Myers Squibb (Princeton, NJ)
    …+ Review/develop site and CRA training materials and presentation at SIV and Investigator meetings and support on Study committee (eg, safety review) activities. + ... knowledge of GCP/ICH, drug development process, study design, statistics, clinical operations . + Proficient knowledge and skills to support program specific data… more
    Bristol Myers Squibb (05/14/25)
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