• Clinical Research Manager - (Women's…

    UPMC (Pittsburgh, PA)
    …disease center program including but not limited to the supervision of Clinical Research Coordinators, Research Associates, and Research Data Coordinators. The ... required. + Prior supervisory/ management experience is required. + 5 years of clinical research experience with a preferred degree. + Must be able to demonstrate… more
    UPMC (12/12/25)
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  • Oncology Late Stage Clinical Scientist…

    Pfizer (Collegeville, PA)
    …supports preparations for Health Authority meetings, participates as appropriate. + Set the clinical data review strategy and leads the team in the collection ... of quality data and review of emerging clinical data and trends; reviews and queries...global regulations. + Extensive understanding of related disciplines, eg, Clinical Operations, Safety, Biostatistics, Regulatory, Study Management ,… more
    Pfizer (11/16/25)
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  • Clinical Drug Supply Manager

    ICON Clinical Research (Blue Bell, PA)
    …of drug returns to 3rd party vendor. Expiry Management + Monitors IP expiry data and informs Clinical Supply team and Clinical Trial teams of pending ... plans and timelines and overall clinical development plan; Works with clinical logistics management to determine resourcing needs; Provides input to the… more
    ICON Clinical Research (11/05/25)
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  • Nurse Clinical Care Coordinator -Allegheny…

    UPMC (Pittsburgh, PA)
    …gaps in preventive care, addresses barriers to care, and supports the member's self- management of chronic illness based on clinical standards of care. ... instrumental activities of daily living. Review UPMC Health Plan data and EMR data , and documentation in...insurance experience preferred. + 1 year of experience in clinical , utilization management , home care, discharge planning,… more
    UPMC (12/31/25)
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  • Senior Clinical Research Associate/…

    Parexel (Harrisburg, PA)
    …+ When required Partners with other Study Team members (eg Clinician, Recruitment Specialist, Clinical Data Scientist) + May act as a Mentor for Clinical ... Clinical Research Associate (Sr. CRA) is responsible for the site management , site monitoring and close-out of assigned clinical trials investigator sites… more
    Parexel (12/07/25)
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  • Clinical Research Coordinator A/B/C

    University of Pennsylvania (Philadelphia, PA)
    …help with study start-up activities. The CRC B will have less supervision in the management of clinical trials and will need to use more independent judgment. ... forms, and research charts. Collect, review, and report study data . Complete case report forms and resolve data...and queries with input from a supervisor as required. Management of clinical trials and will need… more
    University of Pennsylvania (01/01/26)
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  • Clinical Research Nurse Project Manager…

    University of Pennsylvania (Philadelphia, PA)
    …and manage active study invoicing as appropriate. + Provide direct supervision & management to Clinical Research Coordinator(CRC)s within the assigned team and ... valid, accurate study data within the timelines specified by protocol or Clinical Trials Agreement. Coordination may also include clinical activities such as… more
    University of Pennsylvania (11/25/25)
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  • Supervisor, Clinical RN -Med/Surg Nursing…

    Guthrie (Sayre, PA)
    …support staff, exhibiting the Core Values in all activities. Mentors under the Clinical Manager / Director and pursues management and leadership training within ... informed of clinical issues, triage problems, staffing issues, and risk management concerns. Acts on behalf of nurse Manager / Director in his/her absence..… more
    Guthrie (12/25/25)
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  • Supv, Asst Clinical Manager

    Guthrie (Towanda, PA)
    …support staff, exhibiting the Core Values in all activities. Mentors under the Clinical Manager / Director and pursues management and leadership training within ... conjunction with Charge Nurse / Nurse Manager, analyzing available data sources, and making decisions based on this ...clinical issues, triage problems, staffing issues, and risk management concerns. + Acts on behalf of Clinical more
    Guthrie (10/15/25)
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  • Director, Global Clinical Program Leader,…

    CSL Behring (King Of Prussia, PA)
    …Forms (ICF), Medical Monitoring Plans (MMP), Safety Review Committee (SRC)/Independent Data Monitoring Committee (IDMC) Charters, and Clinical Study Reports ... development experience is expected including experience of study data review/evaluation in a pharmaceutical or clinical ...skills including risk mitigation + * Proficient in project management terminology and processes to drive clinical more
    CSL Behring (12/04/25)
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