• Principal Thought Leader Liaison

    Cook Medical (Pittsburgh, PA)
    …thought leaders within the organization, ensuring their input is integrated into the development of the company's clinical, regulatory , and product strategies * ... thought leaders within the organization, ensuring their input is integrated into the development of the company's clinical, regulatory , and product strategies *… more
    Cook Medical (10/07/25)
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  • Senior Program Manager - Toxicology

    WuXi AppTec (Philadelphia, PA)
    …portfolio of services to help global customers and partners shorten the discovery and development timeline and reduce the cost of drug and medical device R&D through ... we provide world-class, globally integrated testing solutions to support drug development . We are committed to helping scientists transform innovative ideas into… more
    WuXi AppTec (09/25/25)
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  • Senior Manager, Medical Writing

    Teva Pharmaceuticals (West Chester, PA)
    …well as resource management for direct medical-writing support in producing clinical research documentation used in drug development and product registrations. ... to make a difference with. **The opportunity** The Senior Manager in Global Regulatory Medical Writing writes and edits clinical regulatory documents, including… more
    Teva Pharmaceuticals (08/09/25)
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  • Nuclear Engineer 3

    Pacific Northwest National Laboratory (Harrisburg, PA)
    …Division, within the National Security Directorate, works across fundamental science, research and development , and operations to counter emerging national ... the Lab, focused on a specific area of scientific research or other function, with its own leadership team...waste, and long-term performance of waste forms. Supports nuclear regulatory work, risk-informed nuclear regulatory analysis, and… more
    Pacific Northwest National Laboratory (10/01/25)
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  • Manager, Medical Writing (Remote)

    Teva Pharmaceuticals (West Chester, PA)
    …and guidance, and managing resources for medical writing support in clinical research documentation used in drug development and product registration. **Travel ... with. **The opportunity** The Medical Writing Manager in Global Regulatory Medical Writing is responsible for writing and editing...life sciences or related field + Preferred: Master's, MD, PhD , PharmD Experience: + Required: 5+ years of relevant… more
    Teva Pharmaceuticals (09/26/25)
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  • Senior Specialist, Quantitative Pharmacology…

    Merck (West Point, PA)
    …the job, you will begin to develop a comprehensive understanding of global regulatory expectations of drug and vaccine development , including clinical trial ... Disease, Nonlinear Mixed Effects Modeling (NONMEM), NONMEM, Phoenix WinNonlin, Regulatory Approvals, Small Molecules, Vaccine Research Current Employees… more
    Merck (10/09/25)
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  • Senior Responsible AI Data Scientist

    Humana (Harrisburg, PA)
    …legal, compliance, education, and IT. In this role, you will contribute to both research and development (R&D) and software development efforts while ... AI systems to ensure ongoing compliance with ethical and regulatory standards. + Stay current with emerging research...PhD in a quantitative field. + Proficiency in development of Python software tools and applications for data… more
    Humana (09/26/25)
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  • Medical Safety Specialist II - Bilingual…

    Olympus Corporation of the Americas (Center Valley, PA)
    …& Scientific Affairs as well as Infection Prevention & Control, Quality Affairs & Regulatory Affairs, Research & Development , Legal, and Health Care ... CFR Part 803, 806, 820) + Various standards (GCP, ISO 13485, ISO 14971) + Regulatory filings (FDA IDE, 510K, EU-MDR CERs, SSCP, PMCFs, PSURs) + Corrective Actions -… more
    Olympus Corporation of the Americas (07/24/25)
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  • Associate Director, RWE Statistics

    Teva Pharmaceuticals (West Chester, PA)
    …Real-World Data (RWD) and other data sources to support lifecycle drug development . The key responsibilities include statistical input to the evidence generation ... planning, medical affairs and RWE research proposal reviews, study protocol and statistical analysis plan (SAP) development and execution, results… more
    Teva Pharmaceuticals (10/02/25)
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  • Medical Director, Global Medical Affairs, Early…

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …- T1) or early development (phase 1) assets either within Medical Affairs, Regulatory Affairs, or Clinical Development is preferred. + Minimum of 7+ years of ... which is comprised of a strong portfolio of individual development and marketed assets. As we continue to develop...and strong competency with the US healthcare system and regulatory landscape is required for this role. + Stay… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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