• Clinical Research Coordinator B/C

    University of Pennsylvania (Philadelphia, PA)
    …spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different interventions and varying complexities. Research coordinator ... study data and regulatory files per GCP. + Work with Regulatory Affairs Specialist to prepare for audits, review regulatory binders, perform internal audit and other… more
    University of Pennsylvania (11/12/25)
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  • Clinical Research Coordinator A/B/C

    University of Pennsylvania (Philadelphia, PA)
    …wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying complexities. Research ... a wide spectrum of clinical trials ranging from phase I to IV, investigator and industry initiated, different disease states and varying complexities. Involvement in… more
    University of Pennsylvania (10/02/25)
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  • Clinical Research Coordinator B

    University of Pennsylvania (Philadelphia, PA)
    …support the fast-paced day-to-day operations of multiple clinical trials, investigator -initiated studies, and translational biobank projects focused on dermatologic ... research environment alongside a team of study coordinators, a regulatory specialist , project managers, investigators, and clinical staff to advance the dermatology… more
    University of Pennsylvania (12/10/25)
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  • Associate / Medical Director - Rheumatology…

    Parexel (Harrisburg, PA)
    …with feasibility leaders, solution consultants + Participate in team project and investigator meetings + Provide training of study teams on TA indication and ... sets, publications etc. Skills * Experience in clinical medicine (general or specialist qualifications) with a specialty Fellowship in a "therapeutic area" which is… more
    Parexel (10/11/25)
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  • Associate Director, Regulatory

    University of Pennsylvania (Philadelphia, PA)
    …and mentor any reporting Regulatory Affairs Supervisor and/or Regulatory Affairs Specialist A/B/C. In this capacity, the Associate Director for Regulatory Affairs ... other University Departments.They will assist with the development of investigator -initiated research protocols and development/maintenance of study specific case… more
    University of Pennsylvania (10/09/25)
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  • Senior AML Consultant

    Deloitte (Pittsburgh, PA)
    AML Project Delivery Specialist -Project Delivery Specialist - Regulatory, Risk & Forensic Operate Are you an experienced, passionate pioneer in technology who ... wants to work in a collaborative environment? As an experienced AML Project Delivery Specialist you will have the ability to share new ideas and collaborate on… more
    Deloitte (12/13/25)
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  • LCMS Laboratory Manager 1

    System One (Pittsburgh, PA)
    …contract to hire Hours: 8AM-5PM Start: Jan Overview: Join as a Research Specialist to perform a variety of independent and complex laboratory work and experiments. ... visualization software applications that will be sent to the primary investigator . + Additional primary duties will include monitoring, maintaining, and… more
    System One (12/14/25)
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  • Senior Medical Writer - US - FSP

    Parexel (Harrisburg, PA)
    …to regulatory authorities, including but not limited to: briefing documents, investigator brochures, study protocols, model informed consents, interim and final ... Supervise collection of documentation by Medical Writing Support Coordinator, Document Specialist , and/or Associate Medical Writer for assembly of project files and… more
    Parexel (12/13/25)
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  • Medical Director - Ophthalmology

    Parexel (Harrisburg, PA)
    …**Knowledge And Experience** + Experience in clinical medicine (general or specialist qualifications) with Fellowship or specialty training in **Ophthalmology** , ... + Experience as a Physician in Industry or as a clinical trial investigator is required + Previous CRO experience is strongly preferred + Medically qualified… more
    Parexel (11/23/25)
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  • Global Development Lead, Internal Medicine

    Pfizer (Collegeville, PA)
    …and regulatory activities including product labels, core data sheets, Investigator Brochures, Development Safety Update Reports, and Periodic Benefit-Risk Evaluation ... + Cardiology, endocrinology, nephrology, internal medicine, or obesity medicine specialist with drug development experience across all Phases of development.… more
    Pfizer (11/05/25)
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