• Program Lead II, Clinical Program Development

    AbbVie (Irvine, CA)
    …colleagues who support clinical trial execution and the Development and Global Medical Affairs Therapeutic Area MDs/SDs. + Key contributor to the ... that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a...Reviews and provides clinical operations content to clinical and regulatory documents (eg, INDs, IB, NDAs, BLAs, MAA, … more
    AbbVie (07/11/25)
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  • Principal Biostatistician FSP, Neuroscience

    IQVIA (Durham, NC)
    …review reports of study results for accuracy. + Support exploratory analyses and medical affairs publications. + Participates in other activities and meetings to ... market rather than project budgets and change orders. + Experience with regulatory submissions. + Engaging, fast-paced environment. + Good work-life balance. **Job… more
    IQVIA (07/10/25)
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  • Risk Management Director

    UNC Health Care (Hendersonville, NC)
    …Legal Employer: Pardee - HCHC Entity: Pardee UNC Health Care Organization Unit: Risk Medical Affairs Work Type: Full Time Standard Hours Per Week: 40.00 Work ... development of a comprehensive patient safety/risk management plan to reduce medical errors, healthcare incidents, and organizational liability. . Identifies areas… more
    UNC Health Care (07/08/25)
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  • Program Manager - Onsite

    Medtronic (Minneapolis, MN)
    …which include matrixed team members from R&D, test, biocompatibility, sterilization, regulatory affairs , operations, supply chain, and quality, among others. ... complex projects and programs in the released product space, including regulatory (ie, MDR) compliance remediation, manufacturing capacity expansion, product design… more
    Medtronic (09/21/25)
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  • Labeling Specialist

    Actalent (San Diego, CA)
    … Device (MD) products. Engage with various departments such as Marketing, Regulatory Affairs , Supply Chain Management, Engineering, Clinical, and Manufacturing ... labeling creators and reviewers with a strong understanding of regulatory standards and guidelines for IVD and MD labeling....for this temporary role may include the following: * Medical , dental & vision * Critical Illness, Accident, and… more
    Actalent (09/19/25)
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  • Clinical Research Coordinator A (Hybrid Eligible)…

    University of Pennsylvania (Philadelphia, PA)
    …study patients as specified per protocol, and the coordinator will also perform regulatory duties such as preparation and submission of regulatory documents ... is an excellent place to get research experience to prepare for medical school or graduate school in psychology, neuroscience, engineering, or biostatistics. Job… more
    University of Pennsylvania (09/17/25)
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  • Clinical Research Coordinator III

    HonorHealth (AZ)
    …limited to coordination team, research nurses, infusion nurses, program managers, and regulatory affairs personnel. Tracking and reporting of weekly workload & ... area. The comprehensive network encompasses six acute-care hospitals, an extensive medical group with primary, specialty and urgent care services, a cancer… more
    HonorHealth (09/17/25)
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  • Director, Global Value Evidence Operations

    Otsuka America Pharmaceutical Inc. (Montpelier, VT)
    …+ Develop and maintain relationships with key functions involved in GVE (eg, Medical Affairs , Market Access, Data and Analytics) and promote interaction between ... build a culture of continuous improvement. + Stay current with global regulatory and compliance requirements related to evidence generation and data use.… more
    Otsuka America Pharmaceutical Inc. (09/13/25)
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  • Core Care Lead

    Sanofi Group (Cambridge, MA)
    Medical Science Liaisons; in addition to home office-based colleagues in Marketing, Medical Affairs , Sales and Market Access. Behaviors that are critical for ... interactions are on-label and consistent with commercial compliance, legal and regulatory guidelines. **Chapter Engagement and Advocacy Development** + Align with… more
    Sanofi Group (09/13/25)
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  • Finance Manager

    University of North Carolina- Chapel Hill (Chapel Hill, NC)
    …trials design, clinical trials data management, and new drug and laboratory testing regulatory affairs . Additionally, as the direction of NIAID , the Network ... the current/projected fiscal environment. They will ensure grant financial and regulatory compliance, manage contracts and subawards and supervise financial staff.… more
    University of North Carolina- Chapel Hill (09/12/25)
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