• Director, Scientific Patient Engagement & Advocacy…

    Merck (North Wales, PA)
    …of best practices in those areas + US/Global experience in clinical research, regulatory affairs , scientific and medical affairs , or pharmaceutical policy ... , Oncology, Patient Advocacy, Patient Insights, Pharmaceutical Industry, Pharmaceutical Medical Affairs , Relationship Management, US Regulatory Affairs more
    Merck (11/21/25)
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  • Senior Clinical Director Ambulatory

    Penn Medicine (Philadelphia, PA)
    …and skill validation of clinical staff . Quality, Patient Safety, and Regulatory Affairs : Partnership with the Vice Chair for Quality, Medical Director ... alignment with Health System Requirements. In conjunction with the Vice-Chair of Regulatory Affairs , develop programs that enhance the clinical decision-making,… more
    Penn Medicine (11/06/25)
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  • Regional Operations Manager, Onc (RN) - Medical…

    UPMC (Pittsburgh, PA)
    …agencies. Responsibilities include the management of operations, quality management, regulatory affairs , continuing education, and fiscal responsibilities. ... to our network offices by partnering with current clinical staff and leadership in each area. They will also...department and Network. Prepares periodic reports as necessary + Regulatory Affairs Management A. Ensures all activities… more
    UPMC (11/12/25)
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  • Assistant Director Government Relations

    Penn Medicine (Philadelphia, PA)
    …Jersey, and Delaware. Reporting to the Senior Director of Government Relations and Regulatory Affairs , the Associate Director helps develop and implement Penn ... Serves as an advisor to the Senior Director of Government Relations and Regulatory Affairs on strategic initiatives and short- and mid-term planning activities,… more
    Penn Medicine (09/24/25)
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  • Registered Nurse - Plasma Center | Sign-On Bonus…

    BioLife Plasma Services (Pittsburgh, PA)
    …emergencies as outlined in SOPs * Refer to the Center Physician or Medical Affairs for guidance on medical or technical issues * Support Hepatitis B and Seasonal ... applying advanced knowledge of emergency care. * Ensures compliance with regulatory standards for plasma collection and maintains detailed documentation. * Manages… more
    BioLife Plasma Services (11/14/25)
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  • Executive Director - Non-Clinical Safety…

    Organon & Co. (Plymouth Meeting, PA)
    …cross-functional interactions with early clinical development, late-clinical development, regulatory affairs , safety and pharmacovigilance, Chemistry, ... Lead will be responsible for ensuring the fulfillment of regulatory requirements and commitments as well as execution of...Manufacturing and Controls (CMC), medical affairs and business development are critical to the success… more
    Organon & Co. (11/18/25)
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  • Medical Director, Clinical Research

    J&J Family of Companies (Spring House, PA)
    …partnership with the Compound Development Team (CDTL) and project management, global regulatory affairs , clinical pharmacology, health economics, and the disease ... Mindset, Drug Discovery Development, Industry Analysis, Innovation, Market Research, Regulatory Affairs Management, Research Ethics, Scientific Evaluation,… more
    J&J Family of Companies (11/12/25)
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  • Clinical Research Coordinator B/C (Abramson Cancer…

    University of Pennsylvania (Philadelphia, PA)
    …subject recruitment, detailed data entry, subject visits, and follow-up and regulatory documentation. The successful candidate will comply with all policies relating ... to the University of Pennsylvania, Penn Medicine, FDA, GCP and other regulatory standards. The Clinical Research Coordinator (CRC) is an integral and essential… more
    University of Pennsylvania (11/02/25)
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  • Clinical Research Coordinator B

    University of Pennsylvania (Philadelphia, PA)
    …tests in EPIC/Pennchart, Radiology, and other research systems; preparing and processing regulatory documents for submission to the IRB, and all regulatory ... Clinical Research Division. Organize and maintain study documentation, preparing and processing regulatory documents for submission to the IRB, and all regulatory more
    University of Pennsylvania (11/15/25)
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  • Clinical Research Coordinator A/B/C (Neurosurgery)

    University of Pennsylvania (Philadelphia, PA)
    …multiple clinical trials. Primary responsibilities will include the following clinical, regulatory and budgetary duties: 1. Clinical: Recruit and assess research ... charts into online databases, data entry and management 2. Regulatory - preparation, submission and monitoring of human subject's protocols,...Will supervise the execution of the trial with the staff to ensure adherence to the protocol is followed… more
    University of Pennsylvania (09/18/25)
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