• Sr. Scientist, Statistical Programming- PKPD…

    Merck (North Wales, PA)
    …Engineering or related field plus 5-9 years SAS programming experience in a clinical trial environment + MS in Computer Science, Statistics, Applied Mathematics, ... related field plus 3-7 years SAS programming experience in a clinical trial environment **Department Required Skills and Experience:** + Effective interpersonal… more
    Merck (08/26/25)
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  • Associate Principal Scientist, Statistical…

    Merck (North Wales, PA)
    …Engineering or closely related field plus 9 years SAS programming experience in a clinical trial environment + OR a Master's degree (or US equivalent) in ... related field plus 7 years SAS programming experience in a clinical trial environment. **Requirements:** + Experience and knowledge in leading large and/or… more
    Merck (09/03/25)
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  • Oncology Regional Medical Scientific Associate…

    Merck (Harrisburg, PA)
    …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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  • Lead Pharmacovigilance QC Specialist

    United Therapeutics (Harrisburg, PA)
    …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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  • Senior Manager, CQA Auditor

    Sanofi Group (Swiftwater, PA)
    …Assurance and/or in Clinical Trials such as Monitoring or Clinical Trial Management + Extensive working knowledge of international ... Assurance and/or in Clinical Trials such as Monitoring or Clinical Trial Management with good performance + Extensive working knowledge of international… more
    Sanofi Group (08/12/25)
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  • Medical Science Liaison, Neuropsychiatry…

    Bristol Myers Squibb (Philadelphia, PA)
    …speakers (if applicable) + Participate in assigned Congress activities **Support Clinical Trial Activities** + Support Interventional and Non-Interventional ... area, competitive landscape and patient treatment trends + Knowledge of clinical trial design and process + Knowledge of the national healthcare and access… more
    Bristol Myers Squibb (08/09/25)
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  • Cardiac Surgery Program Manager (Department…

    University of Pennsylvania (Philadelphia, PA)
    …as the initiation of new clinical trials, which includes negotiation of new clinical trial agreements and associated budgets. The Program Manager will be the ... documents in collaboration with faculty. + Regulatory-Financial-Training/Continuing Education: Negotiate clinical trial agreements and budgets; conduct study… more
    University of Pennsylvania (08/03/25)
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  • Distribution Coordinator

    Catalent Pharma Solutions (Philadelphia, PA)
    …based on-site in Philadelphia, PA. **The Role** + Coordinate and dispatch shipments of clinical trial material to clinical sites. + Process orders, assemble ... in cGMP and FDA regulations is preferred. + Knowledge of exporting clinical trial materials is preferred. + Distribution and cold-chain experience is preferred.… more
    Catalent Pharma Solutions (08/26/25)
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  • Associate Medical Director, Pharmacovigilance…

    Sumitomo Pharma (Harrisburg, PA)
    …marketed products. + Conduct safety surveillance over product life cycle, reviewing clinical trial and post-marketing Individual Case Safety Reports (ICSRs), ... to medical safety of clinical trials, including monitoring of clinical trial safety and laboratory data. + Generates safety queries, evaluates safety data… more
    Sumitomo Pharma (08/15/25)
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  • Pre-Production Manager

    Catalent Pharma Solutions (Philadelphia, PA)
    …labels utilized in packaging and distribution of stability, analytical, commercial, and clinical trial material. The responsibilities include oversight of the ... creation of and control of randomization for clinical trial studies. The scope of this role is the Philadelphia site Pre-Production and Label Control. The… more
    Catalent Pharma Solutions (08/20/25)
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