• Sr. Research Program Coordinator II - #Staff

    Johns Hopkins University (Baltimore, MD)
    …and financial management of clinical trials. + Experience in clinical research and regulatory affairs . + Experience in protocol and informed consent writing, ... of the JH ICU Clinical Trials Group and participating principal investigators (PI). The JH ICU Clinical Trials Group...study documents such as laboratory manuals. + Internally monitor regulatory files and study data to assess compliance, data… more
    Johns Hopkins University (06/14/25)
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  • Director, Clinical Operations

    Bausch + Lomb (Montgomery, AL)
    …global team members, other B&L departments (eg, R&D/Project Management, Clinical/Medical Affairs , Biometrics, Regulatory Affairs , Quality Assurance, ... in an accurate and timely manner. + Provide Clinical Operations support to the Regulatory Affairs department. Leadership: + Manage in-house team of CRAs, CTAs… more
    Bausch + Lomb (09/06/25)
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  • Clinical Research Nurse B/C

    University of Pennsylvania (Philadelphia, PA)
    …investigational protocols under the supervision of Administrative Director and Principal Investigator. Major responsibilities include but not limited to obtaining ... managing the adverse event reporting process and assisting with the regulatory and financial management of multiple studies. Coordinate several investigational… more
    University of Pennsylvania (08/19/25)
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  • Medical Director, Diagnostic Cardiology

    GE HealthCare (Waukesha, WI)
    …is responsible for defining and overseeing the execution of the Medical Affairs strategies in support of the diagnostic electrocardiography (ECG) business (DCAR) ... technology leaders, and research partners to establish comprehensive Medical Affairs programs. The successful candidate will represent DCAR externally and… more
    GE HealthCare (07/29/25)
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  • Senior Clinical Research Monitor

    Edwards Lifesciences (Austin, TX)
    …and how our products transform patients' lives. As part of our Clinical Affairs team, you'll hone your scientific curiosity and passion for evaluating data to ... pioneering technologies for patients in need. In close partnership with principal investigators, dedicated medical professionals, patient advocacy groups, and … more
    Edwards Lifesciences (08/29/25)
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  • Clinical Research Director - RBD

    Sanofi Group (Cambridge, MA)
    …get started? **Main Responsibilities** + The CRD is expected to be a principal team member within the development group. He/she provides medical and scientific ... other members of the CDST (ie, GPH, CSO PL, regulatory , statistics, and PM) + The CRD will lead...will work in conjunction with the Commercial and Medical Affairs to support the creation of the product value… more
    Sanofi Group (08/25/25)
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  • Research Compliance Coordinator

    Texas A&M University System (Kingsville, TX)
    …Bachelor's degree in a related field such as biology, public health, regulatory affairs , or research administration (or equivalent combination of education ... of two years of related experience in research compliance, research administration, or regulatory affairs in an academic or research setting preferred .… more
    Texas A&M University System (09/06/25)
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  • Associate Director, Statistics

    AbbVie (North Chicago, IL)
    …with experts in multiple disciplines to advance medicines to our patients. Principal Responsibilities: + Provide expertise/lead regulatory submission and product ... drive alignment with functional management. Partner with other functions (Clinical, Regulatory , Patient Safety, or GMA) to create development strategies for assigned… more
    AbbVie (08/08/25)
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  • Clinical Lead, Early Clinical and Experimental…

    Sanofi Group (Morristown, NJ)
    …Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area ... Clinical Operations (EDCO, including Clinical Trial Managers and Data Managers), Regulatory Affairs , Patients Safety & Pharmacovigilance, Therapeutic Area… more
    Sanofi Group (07/29/25)
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  • Research Coordinator I - Gastroenterology

    Dartmouth Health (Lebanon, NH)
    …Electronic Medical Record (EMR) and supports data entry needs of the study. * Regulatory Affairs * Assists with compiling and maintaining essential records and ... (written and orally) between stakeholders. * Assists with communications between principal investigators, regulatory agencies, D-H stakeholders and study… more
    Dartmouth Health (07/29/25)
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