• Clinical Research Coordinator B…

    University of Pennsylvania (Philadelphia, PA)
    …and wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B (Department of Endocrinology,Diabetes and Metabolism) Job ... Profile Title Clinical Research Coordinator B Job Description Summary...doc.(eg, visit guides, source document templates), subject study binders, regulatory binders (hard and electronic version), enrollment log for… more
    University of Pennsylvania (08/25/25)
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  • Regulatory Compliance Specialist

    Houston Methodist (Houston, TX)
    …and processes. The Regulatory Compliance Specialist position maintains documentation for clinical research studies, case report forms and study and ... degree or higher **WORK EXPERIENCE** + Two years of clinical research , regulatory compliance, or...Affairs Certifications (RAPS) **OR** + CCRC - Certified Clinical Research Coordinator (ACRP) **OR** + CCRP… more
    Houston Methodist (07/29/25)
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  • Territory Manager, Acute

    Abbott (Boston, MA)
    …Senior Management, Marketing, Training & Education, Research & Development, Regulatory & Clinical Affairs , Reimbursement, Customer Service, and ... relationships and always shows the highest degree of professional behavior . Clinical and Technical knowledge of Abbott CentriMag Circulatory and Respiratory support… more
    Abbott (08/26/25)
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  • SCI Senior Regulatory Specialist (Hybrid)

    Stanford University (Stanford, CA)
    …a strong team of regulatory experts responsible for the administration and regulatory compliance of clinical research within the university, and ... physicians, research scientists, cell manufacturing experts, and clinical research staff to conduct innovative early...for someone who already has a strong foundation in regulatory affairs and human subjects research more
    Stanford University (08/07/25)
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  • Senior Regulatory Compliance Specialist…

    Houston Methodist (Houston, TX)
    …processes. The Sr Regulatory Compliance Specialist position maintains documentation for clinical research studies, case report forms and study and ... of the following certifications: RAC - Regulatory Affairs Certifications (RAPS) or CCRC - Certified Clinical... Affairs Certifications (RAPS) or CCRC - Certified Clinical Research Coordinator (ACRP) or CCRP -… more
    Houston Methodist (08/16/25)
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  • Biocompatibility & Toxicology Senior Scientist

    DEKA Research & Development (Manchester, NH)
    …The individual in this role will work directly with Research & Development, Regulatory & Clinical Affairs and Quality Engineering to formulate and ... DEKA Research & Development has an immediate opening for...toxicological evaluation strategies that support development objectives and world-wide regulatory approvals. How you will make a difference as… more
    DEKA Research & Development (07/18/25)
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  • Senior Principle Scientist, Regulatory

    Merck (Austin, TX)
    …+ Coordinate regional regulatory strategy and submissions through collaboration with Regulatory Affairs Europe (RAE) and local affiliate teams. + Provide ... brochures + Local registration study protocols for secondary markets + Represent Global Regulatory Affairs on internal committees (eg, DRC, ADT/PDT, EDT, LEAD)… more
    Merck (08/23/25)
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  • Sr. Director - Global Regulatory Lead…

    Lilly (Indianapolis, IN)
    …for people around the world. **Purpose:** The purpose of the Senior Director Global Regulatory Affairs , Global Regulatory Lead (GRL) role is to develop ... and regulatory excellence attributes as described in Global Regulatory Affairs white papers. + Constructivelychallengeteams to reachthebest solutions… more
    Lilly (09/02/25)
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  • Senior Director, Clinical Leader…

    J&J Family of Companies (Titusville, NJ)
    …interactions also includes individuals from project management, TA strategy, global regulatory affairs , finance, legal, quality assurance, quality monitoring & ... emerging from the Team and its affiliates + Assists Regulatory Affairs in the development of drug/device...+ May act as company spokesperson regarding publication of clinical research findings and presentations to relevant… more
    J&J Family of Companies (09/03/25)
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  • Summer Intern, Research & Development…

    Bristol Myers Squibb (New Brunswick, NJ)
    …for improvement early. + **Post-Marketing Oversight:** Ensuring independent quality oversight of Clinical and Post-Marketing Safety, Regulatory Affairs , and ... + Assist in overseeing the quality of Non- Clinical , Product Development, Clinical , Patient Safety, Regulatory Affairs , and Medical Affairs more
    Bristol Myers Squibb (09/13/25)
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