• Director, GCP Audits

    Gilead Sciences, Inc. (Parsippany, NJ)
    …global clinical regulations and guidance. + Support the development of GCP Audit material/insights for quality forums and management reviews. _Training & ... and with senior leadership, on key projects and deliveries supporting quality and compliance. + Demonstrates ability to execute against the strategic and… more
    Gilead Sciences, Inc. (06/27/25)
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  • Senior Manager, Clinical Sciences…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    The Senior Manager, Oncology, Clinical Scientist leads in the development, evaluation, planning and execution of clinical studies and ensures integrity and ... interpretation of study data of a clinical development program. The Senior Manager leads...GCP guidelines as well as applicable SOPs regarding clinical safety + Performs clinical /medical data review,… more
    Regeneron Pharmaceuticals (06/15/25)
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  • Senior Manager Clinical Study Lead…

    Regeneron Pharmaceuticals (Warren, NJ)
    …position in one of our office locations. Fully remote is not eligible._ The ** Senior Clinical Study Lead** (CSL) is expected to operate with high-degree of ... for the global execution of assigned large and/or complex clinical trials from study design, through execution, to study...study design, through execution, to study close out. The Senior CSL is accountable for the study timelines, study… more
    Regeneron Pharmaceuticals (07/30/25)
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  • ( Senior ) Clinical Research…

    IQVIA (Parsippany, NJ)
    …accordance with contracted scope of work and regulatory requirements, ie, Good Clinical Practice ( GCP ) and International Conference on Harmonization (ICH) ... in applying, applicable clinical research regulatory requirements, ie, Good Clinical Practice ( GCP ) and International Conference on Harmonization (ICH)… more
    IQVIA (07/14/25)
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  • Senior Clinical Scientist, Late…

    Bristol Myers Squibb (Princeton, NJ)
    …at work and in their personal lives. Read more: careers.bms.com/working-with-us . The Senior Clinical Scientist reports through the Clinical Science function ... writing, reviewing, adjudication/resolution of cross-functional comments, and ensuring high clinical quality (collaboration with Medical Writing) + Site-facing… more
    Bristol Myers Squibb (08/08/25)
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  • Senior Manager, Data, Analytics and AI…

    Bristol Myers Squibb (Princeton, NJ)
    …The Senior Manager, Data, Analytics and AI Product Engineer- Clinical Data Management, Global Drug Development Information Technology (GDDIT), Data & Analytics ... BMS. **Key Responsibilities:** + Accountable for delivering strategy, planning, and high- quality technology solutions for Clinical Data Management portfolio. +… more
    Bristol Myers Squibb (07/30/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Trenton, NJ)
    …global team members, other B&L departments (eg, R&D/Project Management, Clinical /Medical Affairs, Biometrics, Regulatory Affairs, Quality Assurance, ... GCP and B&L SOPs. + Responsible for the quality of all study-related documentation (eg, Trial Master File,...purposes. **POSITION REQUIREMENTS** **:** + Strong knowledge of Good Clinical Practices ( GCP ), clinical trials… more
    Bausch + Lomb (06/07/25)
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  • Senior Cloud & AI Developer/Engineer

    Bristol Myers Squibb (Princeton, NJ)
    …Read more: careers.bms.com/working-with-us . **Summary:** The position requires an experienced Senior Engineer with a strong focus on cloud native services, AI, ... with expert-level experience in AWS and additional experience in GCP or Azure being a plus. We are looking...Have** + The ideal candidate must be a strong Senior Developer and have experience using AWS services beyond… more
    Bristol Myers Squibb (08/10/25)
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  • Late Stage Oncology Clinical Scientist

    Pfizer (Peapack, NJ)
    **Position Summary** You will provide scientific oversight and support data integrity and quality of clinical trial(s) in support of the development strategy for ... program. + Responsible for scientific oversight, data integrity and quality of the clinical trial(s). + Authors...the side of the sponsor. + Strong knowledge of clinical procedures, ICH guidelines, GCP and familiarity… more
    Pfizer (07/29/25)
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  • Senior Specialist - Retention

    Novo Nordisk (Plainsboro, NJ)
    …+ Delivers all relevant services/tasks in support of the retention planning and quality delivery of clinical trials + Responsible for individual patient ... About the Department The Clinical , Medical and Regulatory (CMR) department at Novo...find better and more innovative ways to improve their quality of life. We're changing lives for a living.… more
    Novo Nordisk (08/10/25)
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