• Daiichi Sankyo, Inc. (Basking Ridge, NJ)
    …alignment with other DS processes, guidelines, and policies, and meet applicable ICH and GCP standards. The Associate Director will also be responsible for ... other research areas centered around rare diseases and immune disorders.Summary The Associate Director , Global Clinical Operations (GCO) Procedural Ownership and… more
    HireLifeScience (07/05/24)
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  • Sr. Manager / Associate Director

    Kelly Services (Burlington, MA)
    **Sr. Manager/ Associate Director - Quality Assurance ** **Burlington, MA** **Direct Hire** **Compensation: $125k-165k base + 10-15% annual bonus** ... function. This individual will report to the Sr. Director of Global GCP /GLP compliance and while...as well as organize and drive performance of the quality assurance system. + Experience in a… more
    Kelly Services (07/04/24)
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  • Associate Director , Global PV…

    Ascendis Pharma (Palo Alto, CA)
    The Associate Director , Global PV Operations reports directly to the Head of Global PV Operations. Under the direction of the Head of Global PV Operations, is ... provide appropriate representation during PV related regulatory inspections or internal quality assurance /corporate compliance audits + Work collaboratively with… more
    Ascendis Pharma (05/10/24)
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  • Associate Director Clinical Study…

    BeiGene (San Mateo, CA)
    The Associate Director (AD) Clinical Study Management leads both indirect and direct reports, external partners, consultants, vendors and external budget to ... effective communication and collaboration with functional area peers including Drug Safety, Quality Assurance and Regulatory Affairs, as well as thought leaders… more
    BeiGene (06/22/24)
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  • Associate Director , Process…

    Gilead Sciences, Inc. (Foster City, CA)
    …their aspirations. Join Gilead and help create possible, together. **Job Description** ** Associate Director , Process Development Lead - Data Science:** Recently, ... (GLP). + Work closely with representatives from Research and Development, Manufacturing, Quality Assurance , Regulatory Affairs, and other departments to ensure… more
    Gilead Sciences, Inc. (06/14/24)
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  • Associate Director Clinical…

    J&J Family of Companies (Jacksonville, FL)
    Associate Director Clinical Logistics - 2406191308W...reach and size for good and strive to put quality eye care within reach of everyone, everywhere. Visit ... and Johnson & Johnson Vision on LinkedIn. **Position Summary** : The Associate Director , Clinical Logistics develops strategies to address complex clinical… more
    J&J Family of Companies (06/10/24)
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  • Senior Director Clinical Trials…

    e CancerCare (Fresno, CA)
    Purpose: The Director , Clinical Trials & Research, for CCARE Physicians, PC, is responsible and accountable for the daily operations and management of staff, of the ... compliance with all regulatory requirements and standards of good practice ( GCP ) related to the conduct of clinical research. Responsibilities/Essential Functions… more
    e CancerCare (05/17/24)
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  • Director , Software Engineering

    Walmart (Bellevue, WA)
    …service operations and technology solutions for Finance, People, and the Associate Digital Experience. **About Team:** The Enterprise People Technology team supports ... that includes service operations and technology solutions for Finance, People, and the Associate Digital Experience. **What you'll do:** + Influence, coach, and be a… more
    Walmart (04/26/24)
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  • Clinical Research Coordinator Associate

    University of Michigan (Ann Arbor, MI)
    …+ Abstract data from the medical record + Review collected data and performed data quality assurance of the collected data. + Create reports on the completeness ... Clinical Research Coordinator Associate /Technician Apply Now **How to Apply** A cover...in all their skills and abilities resulting in high quality work. It is presumed that this position is… more
    University of Michigan (07/06/24)
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  • Clinical Site Monitor

    University of Utah (Salt Lake City, UT)
    …and expert regarding regulatory agency standards governing clinical trials. 7. Conduct quality assurance reviews on non- IIT cancer related clinical trials ... and compliance with applicable regulations, standard operating procedures ( SOP ) and GCP guidelines. The auditor is a member of the Research Compliance Office and… more
    University of Utah (06/06/24)
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  • PS Clinical Site Monitor

    University of Utah (Salt Lake City, UT)
    …Learn more**here** **Responsibilities** **Essential Functions** 1. Oversee, coordinate and conduct quality assurance reviews, including monitor and audit visits ... knowledge regarding federal and state guidance, including Good Clinical Practice ( GCP ). **Problem Solving** Incumbent is responsible for assisting the University… more
    University of Utah (07/04/24)
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  • Myeloma Research Program Manager (Cancer Center)

    University of Pennsylvania (Philadelphia, PA)
    …(CRU)- Myeloma Research Team and indirectly report to the CRU Central - Associate Director of Clinical Research Operations. The successful candidate will work ... quality of research. + The candidate will work closely with the CRU Associate Director of Operations to develop and implement SOP's, report team study… more
    University of Pennsylvania (07/06/24)
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