• Clinical Research Coordinator

    Caris Life Sciences (Phoenix, AZ)
    …+ Candidates should have 1-2 years' experience in a Biorepository setting or Clinical Trial setting + Proficient in Microsoft Office Suite, specifically Word, ... biological science + 3-5 years' experience + Candidates should have experience with clinical trial regulatory documentation or TMF. + Candidates should have a… more
    Caris Life Sciences (01/14/26)
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  • Clinical Research Supervisor (Sarcoma)

    University of Colorado (Aurora, CO)
    …Requisition #:** **38661** **Job Summary:** **Examples of Work Performed by the Clinical ** **Supervisor** **Staff Management 40%:** + Under Manager 's guidance, ... Assigns patient and trials to staff with guidance from Clinical Research Manager . + Supervises team vacation,... Clinical Research Professional + CCRA - Certified Clinical Research Associate **Condition of Employment:** +… more
    University of Colorado (01/14/26)
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  • Supervisor, Clinical Research

    University of Miami (Miami, FL)
    …3. Demonstrates proficiency in utilizing research databases and systems including the Clinical Trial Management System (CTMS), Document Management System (DHS), ... a team on special projects and initiatives assigned by Manager . 6. Attends/leads assigned committees/projects, ensuring that assignments and...of Clinical Research Professionals or Society of Clinical Research Associate is required. If the… more
    University of Miami (12/20/25)
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  • Associate Director, Established Brands

    Bristol Myers Squibb (Princeton, NJ)
    … Overview for Type II variation and coordinate expert reports. + Provide clinical trial expertise for existing evidence generation studies or health-authority ... Read more: careers.bms.com/working-with-us . **Position Summary:** The Established Brands Associate Director, Medical Affairs, is responsible for leading and… more
    Bristol Myers Squibb (01/12/26)
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  • Associate Director, Quantitative…

    Regeneron Pharmaceuticals (Tarrytown, NY)
    We are seeking a highly motivated Associate Director (AD) to join the Quantitative Pharmacology (QP) group. The AD will lead model-informed drug development ... combines scientific depth with cross-functional leadership to inform dose selection, trial design, and regulatory strategy from early development through submission.… more
    Regeneron Pharmaceuticals (11/15/25)
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  • Senior Clinical Specialist, Pelvic Health

    Medtronic (San Antonio, TX)
    …resume._ + High School Diploma or GED AND a minimum of 8 years of patient care/ clinical experience; or + Associate 's Degree AND a minimum of 6 years of patient ... + Clinical skill and knowledge (ex. ability to conduct a simple trial , implant and/or refill a pump) + Clinical experience with implantable Neuromodulation… more
    Medtronic (01/16/26)
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  • Clinical Research Nurse

    HCA Healthcare (Nashville, TN)
    …+ **Knowledge of medical and research terminology** + **Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel** ... and integrity. We care like family! Jump-start your career as a Clinical Research Nurse today with TriStar Centennial Medical Center. **Benefits** TriStar Centennial… more
    HCA Healthcare (11/19/25)
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  • Clinical Research Nurse

    HCA Healthcare (Port Charlotte, FL)
    …(GCP) + Knowledge of medical and research terminology + Computer skills including use of clinical trial database, electronic data capture, and MS Word or Excel + ... purpose and integrity. We care like family! Jump-start your career as a Clinical Research Nurse today with HCA Florida Fawcett Hospital. **Benefits** HCA Florida… more
    HCA Healthcare (11/12/25)
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  • Pharmacist (Facility Program Manager )…

    Veterans Affairs, Veterans Health Administration (Anchorage, AK)
    Summary The Clinical Pharmacist Procurement/Pharmacoeconomics Program Manager must have specialized knowledge regarding pharmacoeconomic program development, ... Ensure special labeling and storage and automation, drug file or clinical reminders are set appropriately for High Alert, Look-alike-Sound-Alike, Hazardous,… more
    Veterans Affairs, Veterans Health Administration (01/14/26)
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  • AD, Regulatory Project Manager

    Boehringer Ingelheim (Ridgefield, CT)
    …Authorization Application (MAA) submission, including Health Authority (HA) interactions, Clinical Trial Application (CTA) submissions, Development Safety Update ... and commercialization documents for assigned projects (eg, development plans, protocols, clinical trial reports, CTAs, pediatric development plans and… more
    Boehringer Ingelheim (01/17/26)
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