• Pathologist

    IQVIA (Valencia, CA)
    …laboratory as part of a team. + Provide pathologist input to discussions with clinical trial sponsors to ensure efficient and cost-effective delivery of ... clinical trial goals. + Maintain professional qualifications and accreditations in line with relevant authorizing bodies and continuing professional development.… more
    IQVIA (08/14/25)
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  • Sr Manager, Biostatistics

    Gilead Sciences, Inc. (Foster City, CA)
    …timelines. This may include, but is not limited to, providing statistical consultation on clinical development plans, clinical trial design and clinical ... and analyzes safety reporting, biomarker analyses and other aspects of clinical trial monitoring. + Uses a variety of advanced statistical software, methods,… more
    Gilead Sciences, Inc. (08/13/25)
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  • Medical Science Liaison - West

    IQVIA (Los Angeles, CA)
    …pipeline to investigators in company-sponsored interventional research. + Engage with clinical trial site investigators and staff to understand ... the site and client to find potential medical solutions. Aiming to support clinical trial enrollment. + Provide support to company clinical development and… more
    IQVIA (08/08/25)
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  • Sr Medical Science Liaison, Selution (West Region)

    Cordis (Irvine, CA)
    …support the dissemination of key messages + Present at internal meetings any relevant clinical trial data and facilitate the understanding of trial outcomes ... required 2. Strong knowledge of drug-eluting technologies, vascular biology, and clinical trial methodology. 3. Experience supporting product launches and… more
    Cordis (07/18/25)
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  • Oncology Regional Medical Scientific Associate…

    Merck (Sacramento, CA)
    …and retention efforts to achieve study milestones + Upon request from Global Clinical Trial Operations (GCTO), + Recommends study sites and identifies potential ... License:** Yes **Hazardous Material(s):** n/a **Required Skills:** Advisory Board Development, Clinical Engagement, Clinical Trial Support, Gastrointestinal… more
    Merck (08/23/25)
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  • Research Administrator

    University of Southern California (Los Angeles, CA)
    …projects, including contracts, grants, clinical trials, and philanthropic funding. + Clinical Trial Administration: Manage financial aspects of clinical ... in a fast-paced academic environment + 5+ years of experience in clinical trial financial management + Experience with USC systems, including Workday, Cayuse,… more
    University of Southern California (06/27/25)
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  • Budgeting Specialist - Industry Trials

    University of Southern California (Los Angeles, CA)
    …of the faculty, students and staff that make the university what it is. USC Clinical Trial Office (CTO) is seeking a budget specialist with experience in the ... that all costs and subject reimbursement terms are appropriately captured in the clinical trial agreement. All budgets are developed within the clinical more
    University of Southern California (07/30/25)
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  • Data Management Lead

    Parexel (San Francisco, CA)
    …7+ years experience in pharmaceutical/biotech clinical data management / Biometrics ( clinical trial data and/or Real World Data) + Medical affairs experience ... leading DM study teams, overseeing trial data activities, and collecting clinical trial and/or Real World Data, with a good understanding of molecule and… more
    Parexel (07/02/25)
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  • Lead Pharmacovigilance QC Specialist

    United Therapeutics (Sacramento, CA)
    …experience in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports), OR + Master's Degree in ... in pharmacovigilance in either case processing or quality assurance of ICSRs ( clinical trial cases & post-marketing reports) + 3+ years of experience in vendor… more
    United Therapeutics (08/21/25)
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  • Medical Director, (MD) Padcev

    Pfizer (South San Francisco, CA)
    …Padcev program. This individual contributor position will be responsible for supporting clinical trial (s). The successful candidate should ideally have prior ... authorities. + Lead and contribute to development and maintenance of clinical trial and regulatory documents, in collaboration with Clinical Scientist… more
    Pfizer (08/29/25)
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