• Merck & Co. (Rahway, NJ)
    …- Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. - Preferred Experience and Skills: - - Proficiency ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance Los Angeles Residents… more
    HireLifeScience (03/13/25)
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  • Associate Director , Clinical…

    Regeneron Pharmaceuticals (Basking Ridge, NJ)
    We are seeking an Associate Director to join out Oncology Clinical Development department. The Associate Director Clinical Sciences leads in the ... of study data of a clinical development program. The Associate Director leads in a matrix environment...compliance in accordance with FDA, EMEA, ICH and GCP guidelines as well as applicable SOPs regarding clinical… more
    Regeneron Pharmaceuticals (01/29/25)
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  • Associate Director , Therapeutic…

    Bristol Myers Squibb (Princeton, NJ)
    …in their personal lives. Read more: careers.bms.com/working-with-us . **Position Summary** The Associate Director , Therapeutic Area Audit Strategy Lead will be ... the central QMS team + Lead the Quality and Compliance R&D Escalation Process + Ensure GLP systems are...of vendors and manage external Quality Systems + Execute GCP and Pharmacovigilance audits and support GCP more
    Bristol Myers Squibb (03/20/25)
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  • Associate Director , Clinical Trial…

    Lilly (Branchburg, NJ)
    …better for people around the world. The Clinical Trial (CT) Supply Chain Associate Director will provide operational leadership of clinical supply chain data, ... review, and/or approve appropriate documents outlined in business processes. o Maintain GMP/ GCP compliance . o Reach across boundaries and integrate information… more
    Lilly (03/19/25)
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  • Associate Director , Quality Risk…

    Bristol Myers Squibb (Princeton, NJ)
    …and in their personal lives. Read more: careers.bms.com/working-with-us . Position Summary The Associate Director , RBQM - HOCT, ICN will mainly be responsible ... vendors, demonstrating effective risk and issue management. Provide quality and compliance consultation to clinical trials teams throughout study lifecycle and… more
    Bristol Myers Squibb (03/20/25)
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  • Associate Director for Architecture,…

    Merck (Rahway, NJ)
    …practice,** **drive technology optimization, align teams to overall Security and Compliance Strategy and drive technology and architecture blueprints re-use. The ... IAM, Network Security, Endpoint Security, Security Operations, Risk and compliance ** **Strong Grasp of Architectural Principles and Technologies:** **Deep… more
    Merck (03/20/25)
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  • Associate Director , Clinical Supply…

    Merck (Rahway, NJ)
    …+ Knowledge of Good Manufacturing Practices (GMP) and Good Clinical Practices ( GCP ) is highly desirable. **Preferred Experience and Skills:** + Proficiency in using ... consider qualified applicants with arrest and conviction records for employment in compliance with the San Francisco Fair Chance Ordinance **Los Angeles Residents… more
    Merck (03/14/25)
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  • Associate Clinical Project Management…

    IQVIA (Linden, NJ)
    …delivery, ensuring consistent use of study tools and training materials and compliance with system updates, standard processes, policies and procedures. * Serve as ... and skill in applying applicable clinical research regulatory requirements ie ICH GCP and relevant local laws, regulations and guidelines, towards clinical trial… more
    IQVIA (03/06/25)
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