• Associate Director , Advertising…

    Merck (North Wales, PA)
    **Job Description** Reports to the Director /Senior Director in the Office of Promotion and Advertising Review (OPAR) The Associate Director is responsible ... and approval of all US promotional materials and serving as the promotional regulatory expert with marketing, legal, and medical teams to ensure that promotional… more
    Merck (09/07/24)
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  • National Director , Field Medical…

    Inovio Pharmaceuticals (Plymouth Meeting, PA)
    …Science Liaison (MSL) and Clinical Device Liaison (CDL) teams. The National Director , Field Medical Affairs (FMA) will report to the VP of Medical ... more information, visit www.inovio.com . Job summary The National Director , Field Medical Affairs (FMA) will be...Ensures field compliance of all relevant corporate policies and regulatory guidelines. + Ensure all Field Medical materials and… more
    Inovio Pharmaceuticals (07/24/24)
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  • Associate Director , US Advertising…

    Takeda Pharmaceuticals (Exton, PA)
    …of proposed promotional and disease state materials. + Collaborate with Regulatory Affairs , Medical, Legal, Commercial, and Compliance, execute and ... my knowledge. **Job Description** Join Takeda as an Associate Director , US Advertising & Promotion Regulatory Review... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
    Takeda Pharmaceuticals (09/06/24)
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  • Senior Medical Science Liaison

    Cardinal Health (Trenton, NJ)
    …education for healthcare professionals, patients and others. This role reports to the Director of Regulatory & Medical Affairs . **Responsibilities:** + ... three hours. We give customers the support they need in regulatory compliance, reimbursement, continuing education, information management and other crucial areas,… more
    Cardinal Health (08/31/24)
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  • Senior Manager, US Medical Ad/Promo…

    Takeda Pharmaceuticals (Exton, PA)
    …potential issues. POSITION ACCOUNTABILITIES: + Collaborate with colleagues in Regulatory Affairs , Medical, Legal, Commercial, and Compliance organizations ... the US Medical team, you will report to the Director , Ad/Promo Regulatory Review. You will be... regulatory requirements. + Understand broad concepts within Regulatory Affairs and potential effects across the… more
    Takeda Pharmaceuticals (08/15/24)
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  • Director , Clinical Research Operations…

    University of Pennsylvania (Philadelphia, PA)
    …and wellness programs and resources, and much more. Posted Job Title Director , Clinical Research Operations (Department of Dermatology) Job Profile Title Director ... alignment with the University of Pennsylvania, GCP, FDA and all applicable regulatory bodies. The candidate must have a comprehensive understanding of clinical trial… more
    University of Pennsylvania (07/06/24)
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  • Grants Manager A/B (Dept. of Pathology…

    University of Pennsylvania (Philadelphia, PA)
    …proposals and accounts for compliance with sponsor and University policies and ensure Regulatory Affairs requirements are satisfied and that Conflict of Interest ... A/B. The Grants Manager A/B will report to RBO's Director , Fiscal Operations. PLM's RBO supports the research...for compliance with sponsor and University policies and ensure Regulatory Affairs requirements are satisfied and that… more
    University of Pennsylvania (09/20/24)
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  • Clinical Research Coordinator C (Department…

    University of Pennsylvania (Philadelphia, PA)
    …guidance to both study trials and device trials. The incumbent will be a liaison to departmental interaction such as the investigational team, the nursing units and ... implement a plan of action; will work with the regulatory manager to ensure that submissions to the IRB...provide monthly updates to the research team and the director . This role requires a combination of both comprehensive… more
    University of Pennsylvania (07/03/24)
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  • Clinical Research Operations Manager, Abramson…

    University of Pennsylvania (Philadelphia, PA)
    …Manager position will directly report to the ACC CRU Central - Associate Director of Clinical Research Operations and indirectly to the Physician Leaders of the ... any issues + Collaborate with ACC CRU Central Associate Director of Clinical Research Operations: + Review of Research...research with collaborators. + Work closely with the CRU Regulatory Managers to optimize Regulatory Support for… more
    University of Pennsylvania (08/03/24)
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  • Grants Manager A (Center for Sleep)

    University of Pennsylvania (Philadelphia, PA)
    …these grants. + Review granting agency regulations, inform investigators of regulatory requirements and ensure compliance. + Prepare & maintain confidential ... include salary, budget & proposal information. + Serve as liaison with ORSS and ORS. + Thorough knowledge of...needed. + Assist with close-out of grants. + Assist Director & Sr. Grants Manager with collection of relevant… more
    University of Pennsylvania (07/11/24)
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