• Associate Practice Manager - Cancer Ctr VF

    Penn Medicine (Berwyn, PA)
    …leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across ... supervision and direction in regards to all administrative, financial, regulatory , quality, human resources, patient/employee satisfaction, and clinical aspects for… more
    Penn Medicine (08/07/25)
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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. **Job Duties ... PV Operations on cross-functional program and project teams; support PV Medical Safety activities on cross-functional program and project teams, as required.… more
    Sumitomo Pharma (08/01/25)
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  • Senior Corporate Counsel, Compliance & Commercial

    NASCO (Harrisburg, PA)
    …operates under general direction and is responsible for providing legal and regulatory guidance to the organization. This person negotiates and drafts complex ... structure and associated risks, ensuring alignment with organizational goals and regulatory requirements + Collaborates with business partners on agreement structure… more
    NASCO (06/27/25)
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  • RN Float Pool/Registry (Weekend Program), West…

    Highmark Health (Pittsburgh, PA)
    …safe and effective care for the age population served according to regulatory requirements. Professionally directs and manages the activities of the patient care ... safe and effective care for the age population served according to regulatory requirements. Professionally directs and manages the activities of the patient care… more
    Highmark Health (06/20/25)
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  • Device Engineer I

    Teva Pharmaceuticals (West Chester, PA)
    …grow through design control practices, physical testing, and documentation to support regulatory filings and product quality. **How you'll spend your day** . Perform ... technical reports, data summaries, and documentation for design verification and regulatory submissions. . Collaborate with cross-functional teams including QA, … more
    Teva Pharmaceuticals (08/09/25)
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  • Clinical Services Associate

    Penn Medicine (Philadelphia, PA)
    …leaders in the field of medicine. Working for this leading academic medical center means collaboration with top clinical, technical and business professionals across ... CSA supports the practice by performing clinical and administrative duties as a Medical Assistant and as a Patient Services Associate. The practice will determine,… more
    Penn Medicine (08/07/25)
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  • Senior Director, Global Clinical Development CNS

    Otsuka America Pharmaceutical Inc. (Harrisburg, PA)
    …to post commercialization; with emphasis on the large global clinical trials and regulatory filing activities. The Senior Director, GCD is responsible for all the ... programs, including: + Understanding pharmacology of drugs and unmet medical needs. + Formulating a rationale to develop the...develop the drug in accordance with a clinical and regulatory strategy. + Working with experts and consultants in… more
    Otsuka America Pharmaceutical Inc. (07/16/25)
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  • Director, Aida R&D Advanced AI & Data Ecosystem…

    Pfizer (Collegeville, PA)
    …that supports cross R&D solution delivery, ensuring alignment with scientific goals, regulatory requirements, and enterprise digital strategy. You will lead a team ... understanding of user needs, scientific workflows, developer needs, and any regulatory constraints + Champion agile product development practices and iterative… more
    Pfizer (09/04/25)
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  • Senior Manager, Clinical Project Management

    Sumitomo Pharma (Harrisburg, PA)
    …and vendors, and ensures the documentations are in accordance with GCP regulatory requirements and consistent with the protocol for assigned studies. + Participates ... documents such as protocols, protocol amendments, clinical study reports (CSRs), regulatory submissions and other publications as required. . Participates in… more
    Sumitomo Pharma (09/03/25)
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  • Senior Manager, CQA Auditor

    Sanofi Group (Swiftwater, PA)
    …to corporate standards, study requirements and compliance with applicable regulatory requirements. Non-routine audits may include Due Diligence or for-cause ... secrecy and as such will not disclose any individual identity and/or individual medical information. + During the audit, identifies potential issues and risks with… more
    Sanofi Group (08/12/25)
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