• Associate Principal Scientist

    Organon & Co. (Plymouth Meeting, PA)
    …questions per established business processes and systems. + Demonstrate an understanding of regulatory affairs and apply this understanding to the benefit of the ... **Job Description** **The Position** The Associate Principal Scientist (Associate Director) is responsible for developing and implementing Regulatory Chemistry,… more
    Organon & Co. (07/22/25)
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  • Data Systems Senior Scientist /Sr.…

    Merck (Lower Gwynedd, PA)
    …Computer Science, Data Visualization, Detail-Oriented, Discrete Mathematics, Drug Regulatory Affairs , Employee Training Programs, Global Communications, ... **Job Description** **Job Description** Data Systems Senior Scientist (P3), Regulated Bioanalytics, Integrated Logistics & Sample...Management Process, Pattern Recognition, Pharmaceutical Regulatory Affairs , Pharmacovigilance, Process… more
    Merck (09/16/25)
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  • Associate Director, Global Regulatory

    Organon & Co. (Plymouth Meeting, PA)
    …Teams and regulatory single point-of-contact for products within Global Regulatory Affairs and outside. + Communicate new legislations, guidelines and ... entire life cycle of the drug. + Represent Global Regulatory Affairs within our company's internal committees...review as needed + Act as mentor of Sr Scientist , as required, for specific projects/products. Other Tasks +… more
    Organon & Co. (07/26/25)
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  • Principal Scientist , Translational…

    Merck (North Wales, PA)
    …our Company, collaborating with project teams, biomarker leads, clinical operations, and regulatory affairs on the implementation of global CDx assay strategies ... **Job Description** In this Principal Scientist position within Translational Oncology, this team member will provide leadership for aligned and integrated… more
    Merck (09/22/25)
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  • Senior Principal Scientist , Clinical…

    Merck (North Wales, PA)
    …+ Work closely with a cross-functional group of experts in commercialization, regulatory affairs , statistics, and manufacturing to manage clinical development ... Pulmonary Disease Research, Pulmonary Disease Treatment, Pulmonary Disorders, Pulmonology, Regulatory Affairs Compliance, Regulatory Compliance, Scientific… more
    Merck (09/22/25)
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  • Principal Scientist (Director) - Outcomes…

    Merck (Upper Gwynedd, PA)
    **Job Description** The Principal Scientist /Director, Value & Implementation (V&I) Outcomes Research, position resides in the V&I organization, which includes Global ... Medical and Scientific Affairs as well as Outcomes Research. Under the guidance...reimbursement and market access, and provides input into clinical, regulatory , payer/access, marketing and evidence generation strategies and programs.… more
    Merck (09/17/25)
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  • Senior Director, RWE/Epi Scientist Internal…

    Pfizer (Collegeville, PA)
    …for communications in writing and in presentations to internal stakeholders, regulatory authorities, medical professionals and others. The SD will be accountable ... to ensure strategic input is being provided to IEPs through Global Medical Affairs Teams + Work collaboratively to establish & operationalize processes & systems to… more
    Pfizer (09/27/25)
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  • Oncology Early Stage Clinical Scientist

    Pfizer (Collegeville, PA)
    …and external partners, such as project leaders, research units, biostatistics, regulatory affairs , clinical pharmacology, human genetics, translational oncology, ... clinical study reports (CSRs), investigator brochures, statistical analysis plans, and regulatory documents. + Foster a transparent environment that builds strong… more
    Pfizer (08/21/25)
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  • Manager, PVRM

    Sumitomo Pharma (Harrisburg, PA)
    …but not limited to, Clinical Development, Translational Medicine/Early Development, Regulatory Affairs , Data Management and Biostatistics is essential. ... highly motivated, and experienced individual for the position of Pharmacovigilance Scientist to perform PV activities for assigned programs(s). Ability to work… more
    Sumitomo Pharma (08/01/25)
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  • GCI Ligand Binding Assays Team Lead- Vaccines

    Sanofi Group (Swiftwater, PA)
    …Act transversally (including with global transversal operations, clinical development, global regulatory affairs ) to build and optimize novel bioanalytical ... + 5+ years experience working in a regulated laboratory as a research scientist or laboratory manager preferably in pharma R&D. + Experience in the development… more
    Sanofi Group (09/19/25)
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