• Clinical Affairs , Senior…

    ThermoFisher Scientific (Greenville, NC)
    …Schedule** Standard (Mon-Fri) **Environmental Conditions** Office **Job Description** ** Clinical Affairs , Senior - Study Operations** In this role, ... planning and study execution Additionally, you will analyze clinical affairs operations, identifying areas for improvement and implementing corrective… more
    ThermoFisher Scientific (10/02/25)
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  • Senior /Statistical Scientist - Global…

    United Therapeutics (Research Triangle Park, NC)
    …team and other stakeholders to provide biostatistical resources for investigator-sponsored clinical studies and address internal/external investigator queries of ... input, conduct thorough reviews, and grant approval for submitted investigator-sponsored clinical studies , external investigator queries of UT databases,… more
    United Therapeutics (09/26/25)
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  • Senior /Medical Writer - Global Medical…

    United Therapeutics (Research Triangle Park, NC)
    …creative and detail-oriented with deep expertise in regulatory submissions and writing, including clinical study reports, clinical study protocols, and ... manuscripts, posters, and several regulatory documents including but not limited to: clinical study protocols and reports, Investigator's Brochures, and safety… more
    United Therapeutics (09/05/25)
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  • Senior Project Manager - Global Medical…

    United Therapeutics (Research Triangle Park, NC)
    …successful planning and completion of assigned projects, including clinical studies , registries, or other strategic study /departmental initiatives. + Lead ... for which transplant is not currently an option. The Senior Project Manager of Medical Affairs will...and performance expectations + Serve as primary contact during clinical study /project, including regular collaboration, conferences calls… more
    United Therapeutics (09/26/25)
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  • Physician Assistant - Surgical Services…

    Veterans Affairs, Veterans Health Administration (Durham, NC)
    …PA-IV grade level may serve as clinical leader or administrative leader. Clinical PA Leaders may be assigned to positions/ studies where limited guidance ... may monitor or evaluate services or programs with interaction of senior administration. Experience. PA clinical leaders/administrative leaders require five… more
    Veterans Affairs, Veterans Health Administration (10/16/25)
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  • Associate Director, Regulatory Affairs…

    Sumitomo Pharma (Raleigh, NC)
    …relationships with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, ... general product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
    Sumitomo Pharma (10/11/25)
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  • Director, Regulatory Affairs

    Sumitomo Pharma (Raleigh, NC)
    …relationship with colleagues, fostering collaboration, and idea sharing + Reviews nonclinical, clinical and CMC documentation (eg nonclinical study reports, ... general product development in the pharmaceutical industry + Experience reviewing nonclinical, clinical and CMC documentation (eg nonclinical study reports, … more
    Sumitomo Pharma (09/09/25)
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  • Clinical Quality Operations Manager- FSP

    Parexel (Raleigh, NC)
    …will include ongoing partnership with Client QA and acting as the link between Clinical Development, study teams, global business functions and regional study ... **_Parexel FSP has an exciting opportunity for a Clinical Quality Operations Manager ! This is a...of the quality management system are in place for studies conducted in partnership with non-commercial organizations (eg NGO,… more
    Parexel (10/11/25)
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  • Senior Biostatistician (FSP)

    IQVIA (Durham, NC)
    …and Clinical Operations on design of eCRFs. + Contributes to clinical study reports and other regulatory documents eg, DSURs, Briefing Documents, ... **Job Level:** Senior Biostatistician, FSP **Location:** Home-based in the US...study protocols. + Writes the statistical sections of clinical trial protocols, while consulting with internal and external… more
    IQVIA (08/22/25)
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  • Senior Specialist, Medical Writing

    Edwards Lifesciences (Raleigh, NC)
    …our innovations and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for ... summaries of the data to support the development of clinical evaluation reports and clinical study...with 5 years of related experience working in medical affairs , clinical affairs and/or … more
    Edwards Lifesciences (09/27/25)
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