• Post-Approval Compliance Monitor

    Alaka'ina Foundation Family of Companies (Silver Spring, MD)
    …training, as needed/requested. DESCRIPTION OF RESPONSIBILITIES: The WRAIR-based clinical research scientific monitoring services (Post-Approval Compliance ... three months of TO award and updated annually. + Perform routine and for-cause monitoring of human subjects research and protocols that receive research more
    Alaka'ina Foundation Family of Companies (06/21/25)
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  • Clinical Trial Nurse - Greer

    IQVIA (Greenville, SC)
    …Part time - 48 hours/wk and onsite support.** Coordinate and participate in clinical research studies ensuring that studies are carried out according to ... research support to investigators to prepare for and execute assigned research studies * Reviews study protocols, source document forms, other study-specific… more
    IQVIA (09/06/25)
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  • Nurse Practitioner (Acute Care), Physician…

    Cleveland Clinic (Akron, OH)
    …of the health care team. + Promotes translation of evidence-based practices, guidelines, and research . + May conduct research studies . May assists in data ... day/night and weekend shifts._ _6am-6pm/6pm-6am_ **Responsibilities:** + Conducts thorough medical histories, performs complete physical examinations (where indicated), initiates… more
    Cleveland Clinic (09/12/25)
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  • Oncologist-Developmental Therapeutics |

    Novant Health (Charlotte, NC)
    …and focus, record of regulatory authority interactions, organization of translational research studies , and/or organization of investigator-initiated studies ... Job Summary Medical Director for Oncology Developmental Therapeutics Authorities and...colleagues who may be the PI in early phase studies but collaborate with the Developmental Therapeutics program for… more
    Novant Health (08/21/25)
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  • Principal Clinical Data Science Lead

    ICON Clinical Research (Blue Bell, PA)
    …Colombia ICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation ... team. The Principal CDSL is responsible for managing clinical data science teams, studies , and programs of studies . The Principal CDSL will provide planning… more
    ICON Clinical Research (09/13/25)
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  • Medical Director, Clinical Development…

    AbbVie (North Chicago, IL)
    …may include supervision of matrix team members and serving as Clinical Research representative to lend clinical development and medical expertise to ... standard operating procedures and to all other quality standards in conducting research . Qualifications Qualifications + Medical Doctor (MD), Doctor of… more
    AbbVie (08/13/25)
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  • Medical Technologist I

    ThermoFisher Scientific (Austin, TX)
    …individual career goals while taking science a step beyond through research , development and delivery of life-changing therapies. With clinical trials conducted ... countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio,...support for clinical trials from study start up to monitoring through to study close out, across commercial and… more
    ThermoFisher Scientific (09/10/25)
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  • Clinical Monitor Line Manager

    University of Southern California (San Diego, CA)
    …Extensive clinical research experience, and experience monitoring clinical research studies . Experience with medical terminology, and with the ... for Alzheimer's Disease (AD) through innovative clinical trials. The Medical & Safety team within ATRI is looking for...degree Preferred Experience: 10 years 6 years of experience monitoring clinical research studies . Preferred… more
    University of Southern California (08/29/25)
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  • Associate Director, Clinical Scientist, Hematology

    Regeneron Pharmaceuticals (Tarrytown, NY)
    …conventions across studies /programs; Reviews clinical data review plan and authors medical monitoring plan for assigned studies /program **This role may ... proficient scientific expertise to propose, design, and execute clinical research and development studies for early and/or...Authors and/or reviews documents related to trials, such as medical monitoring plans, SAPs, informed consents and… more
    Regeneron Pharmaceuticals (07/23/25)
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  • Early Development Project Leader

    Sanofi Group (Cambridge, MA)
    …collecting valuable data, managing budgets and timelines + work with medical leads, data managers, statisticians, clinical supplies managers and regulatory affairs ... + contribute to the development of new drugs and medical devices through clinical trials + May be a...operational strategy, implementation and realization of FIM to POC/POCC studies ** based on input from all applicable functions within… more
    Sanofi Group (09/12/25)
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