• AI & Data Manager - Life Sciences R&D…

    Deloitte (Philadelphia, PA)
    …to include: introducing new technologies like GenAI, AI/ML, and automation for pharmaceutical regulatory content or regulatory intelligence; Veeva RIM ... immigration sponsorship may be available Preferred: + Understanding of pharmaceutical regulatory data and regulatory filing requirements and generating… more
    Deloitte (07/09/25)
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  • Senior Specialist, Financial Disclosure US…

    Merck (North Wales, PA)
    …Joint Ventures, Management Process, Manufacturing Compliance, Oral Communications, Pharmaceutical Regulatory Affairs, Pharmacovigilance, Process Improvements, ... Division. Our mission is to serve as a trusted regulatory center of excellence and lead successful interactions with...is an exciting time to join the US Subsidiary regulatory space, as we navigate evolving expectations and drive… more
    Merck (09/06/25)
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  • Clinical Research Regulatory Affairs…

    University of Pennsylvania (Philadelphia, PA)
    …requisite ancillary review committees. + Prepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations ... programs and resources, and much more. Posted Job Title Clinical Research Regulatory Affairs Specialist Job Profile Title Clinical Research Regulatory Specialist… more
    University of Pennsylvania (08/27/25)
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  • Senior Principle Scientist, Regulatory

    Merck (North Wales, PA)
    …Immunotherapy, International Regulatory Compliance, Leadership, Motivation Management, Pharmaceutical Regulatory Affairs, Regulatory Affairs Management, ... **Job Description** The Global Regulatory Liaison is responsible for developing and implementing... Liaison is responsible for developing and implementing worldwide regulatory strategies for assigned projects within the Immunology therapeutic… more
    Merck (08/23/25)
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  • Clinical Research Regulatory Specialist B…

    University of Pennsylvania (Philadelphia, PA)
    …He/she will, with minimal supervision, prepare and process all required regulatory documentation for pharmaceutical companies, contract research organizations ... programs and resources, and much more. Posted Job Title Clinical Research Regulatory Specialist B (Abramson Cancer Center) Job Profile Title Clinical Research … more
    University of Pennsylvania (08/03/25)
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  • Sr. Coordinator, Regulatory Submissions…

    Cardinal Health (Harrisburg, PA)
    …format, edit and compile paper and electronic documents related to the pharmaceutical industry regulatory submissions throughout each phase of drug development ... **_What Regulatory Submissions Operations contributes to Cardinal Health_** Regulatory Submissions Operations uses specialized technology and knowledge to… more
    Cardinal Health (08/15/25)
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  • Director, Regulatory Policy & Intelligence

    Organon & Co. (Plymouth Meeting, PA)
    …or related discipline, or PharmD. with at least five years' experience in Pharmaceutical Industry or Academia. + Regulatory Policy and Intelligence Professional ... **Job Description** **The Position** Leading the Regulatory Policy and Intelligence activities for Global Regulatory Affairs covering all Therapeutic Areas and… more
    Organon & Co. (07/23/25)
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  • Associate Director - CMC Development

    Lilly (Philadelphia, PA)
    …transfer, cGMP manufacturing, analytical development, release, quality control, and regulatory expectations for pharmaceutical products. + Direct experience ... Development, Analytical Sciences, Manufacturing, Quality, Supply Chain, R&D, Finance, and Regulatory to ensure delivery of CMC milestones for priority assets… more
    Lilly (08/12/25)
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  • Distribution Associate, Inbound

    Glenmark Pharmaceuticals Inc., USA (Allentown, PA)
    …experience preferred + Technical capacity with Excel and Outlook + Pharmaceutical Regulatory statues, GMP compliance + Previous Distribution, Inventory ... responsibility for the accurate and compliant handling of inbound and returned pharmaceutical products, ensuring all inbound shipments are received per the Drug… more
    Glenmark Pharmaceuticals Inc., USA (07/18/25)
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  • Clinical Research Coordinator B (Department…

    University of Pennsylvania (Philadelphia, PA)
    …reviews, amendments, and adverse event reporting. + Prepare and process all regulatory documentation with pharmaceutical companies and CROs. + Obtain the ... subject recruitment, detailed data entry, subject visits, and follow-up and regulatory documentation. The successful candidate will comply with all policies relating… more
    University of Pennsylvania (06/16/25)
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