• 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, ... (POC) studies in Oncology. You will work in close collaboration with the Global Development Lead (GDL)and members of the development team to establish, lead,… more
    Pfizer (11/08/25)
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  • Associate Director , Program Manager

    Organon & Co. (Plymouth Meeting, PA)
    …of industry experience​ in R&D functions (eg, Clinical Research, Early Development, Medical Affairs , Pharmacovigilance, Regulatory Affairs , etc.) + At least ... **The Position** We are looking for an experienced Associate Director , Program Manager to join our team. This successful...live their best lives. We are a $6.5 billion global healthcare company focused on making a world of… more
    Organon & Co. (11/04/25)
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  • Director , Computational Multiomics,…

    J&J Family of Companies (Spring House, PA)
    …of internal and external human data resources. + Partner with Clinical Development, Global Regulatory Affairs , Data Science, Patient Reported Outcomes, ... while championing patients every step of the way. We are searching for a ** Director , Computational Multiomics, Neuroscience,** to be located at one of our offices in… more
    J&J Family of Companies (11/18/25)
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  • Director , Supply Chain Clinical Supply…

    Catalent Pharma Solutions (Philadelphia, PA)
    …successful candidate will work closely with Clinical Operations, Quality Assurance, Regulatory Affairs , and the Program Management team. Strong cross-functional ... **Job Description** We are seeking a ** Director in** **Clinical Supply Chain** to be part...offers rewarding opportunities to further your career!** Join the global drug development and delivery leader and help us… more
    Catalent Pharma Solutions (10/29/25)
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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. ... Cancer Center is exceptionally well-positioned to contribute to the global effort to reduce the burden of cancer. UPMC...department and Network. Prepares periodic reports as necessary + Regulatory Affairs Management A. Ensures all activities… more
    UPMC (11/12/25)
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  • Senior Quality Manager

    West Pharmaceutical Services (Williamsport, PA)
    …and manages quality control, quality assurance, quality systems, metrology and/or regulatory affairs , personnel, department resources, and continuous improvement ... processes related to the manufacture of West products. Ensure compliance with regulatory requirements and West procedures. Proactively develop, lead, and drive the… more
    West Pharmaceutical Services (09/30/25)
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  • Head, Dermatology, US Medical Affairs

    J&J Family of Companies (Horsham, PA)
    …with the global functions including clinical R&D, translational medicine, regulatory affairs /labelling, and global medical safety. This includes ... Learn more at https://www.jnj.com/innovative-medicine **Purpose:** The Head, Dermatology, US Medical Affairs - Immunology is a Senior Director role responsible… more
    J&J Family of Companies (10/30/25)
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  • Trial Master File (TMF) Specialist Oncology

    Sumitomo Pharma (Harrisburg, PA)
    …ensure system validation is maintained. + Work closely with Clinical Operations and Regulatory Affairs to ensure compliance with regulatory requirements. + ... Sumitomo Pharma Co., Ltd., is a global pharmaceutical company based in Japan with operations...ready for audits and inspections. Partnering with the Associate Director , Clinical Business Operations, the specialist ensures accountable functions… more
    Sumitomo Pharma (11/05/25)
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  • Medical Safety Specialist II

    Olympus Corporation of the Americas (Center Valley, PA)
    …Medical & Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs , Research & Development, Legal, and Health ... Director Medical Safety as a member of the global medical safety team. You must be adept at...+ Various standards (GCP, ISO 13485, ISO 14971) + Regulatory filings (FDA IDE, 510K, EU-MDR CERs, SSCP, PMCFs,… more
    Olympus Corporation of the Americas (10/23/25)
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