• IRB Specialist I

    AdventHealth (Orlando, FL)
    …or research related experience preferably in an academic or medical setting o Certified Institutional Review Board Professional achieved within two (2) years ... IRB Specialist -I provides training for IRB Office Coordinators, external IRB review...preferably in an academic or medical setting + Certified Institutional Review Board Professional This… more
    AdventHealth (10/25/24)
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  • Regulatory Specialist II

    AdventHealth (Orlando, FL)
    …setting, with at least 2 years in a clinical research setting including an institutional review board office, research administration, or regulatory affairs ... Specialist II functions as a liaison between the IRB of record for each study protocol, the Food...FDA and other regulatory authorities. Assists with the technical review and report preparation and submission of FDA required… more
    AdventHealth (11/12/24)
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  • Research Regulatory Specialist III

    AdventHealth (Orlando, FL)
    …the research regulatory field in a clinical research or scientific setting, an institutional review board office, research administration, or regulatory ... Specialist III functions as a liaison between the IRB of record for each study protocol, the Food...with the FDA and other regulatory authorities. Provides technical review and report preparation and submission of FDA required… more
    AdventHealth (11/13/24)
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  • Clinical Nurse Specialist RN

    AdventHealth (Orlando, FL)
    …nurses who are involved in developing research projects/protocols. Participates with the Institutional Review Board and Nursing Research Council. **The ... registered professional nurse + Current registration with Florida State Board of Nursing as a Clinical Nurse Specialist... Board of Nursing as a Clinical Nurse Specialist + Basic Life Support (BLS) certification + Advanced… more
    AdventHealth (11/12/24)
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  • Clinical Research Coord III

    University of Florida (Gainesville, FL)
    …other body fluids samples per clinical trial protocol *Preparing reports to the Institutional Review Board in a timely manner *Facilitating sponsors/monitors ... regulations regarding research *Communicating with research sponsors, monitoring agencies and the Institutional Review Board (s) in a timely, accurate, and… more
    University of Florida (11/15/24)
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  • OPS - Clinical Research Coordinator I

    University of Florida (Gainesville, FL)
    …research participant recruitment, including human participants protection, health studies and Institutional Review Board SKILLS: Demonstrated expertise in ... to adjust recruitment and retention strategies + Follow an IRB approved protocol and train new research specialist... IRB approved protocol and train new research specialist and students on adhering to the approved … more
    University of Florida (11/19/24)
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  • Clinical Research Participant Specialist

    University of Miami (Miami, FL)
    …staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . The Hussman ... an exciting opportunity for a full time Clinical Research Participant Specialist position. The incumbent assists in community outreach, recruitment, enrollment, and… more
    University of Miami (11/19/24)
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  • Manager, Research Support

    University of Miami (Miami, FL)
    …or supervise the CRCs with process of regulatory document submission to the Institutional Review Boards ( IRB ) including communicating with ancillary ... faculty or staff position using the Career worklet, please review this tip sheet (https://my.it.miami.edu/wda/erpsec/tipsheets/ER\_eRecruiting\_ApplyforaJob.pdf) . Manager, Research Support… more
    University of Miami (10/25/24)
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  • Emergency Medicine Research Faculty - Assistant…

    University of Florida (Jacksonville, FL)
    …a PhD associate director, assistant director of clinical trials, research administrative specialist , IRB and REDCap coordinator, full and part-time clinical ... Department of Emergency Medicine - Jacksonville is seeking a full-time board -certified emergency physician leader with experience in federally funded research and… more
    University of Florida (11/22/24)
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  • Senior Clinical Trial Associate, Oncology

    Sumitomo Pharma (Tallahassee, FL)
    …members with clinical trial execution, eg, development and formatting of documents, review and reconciliation of study- specific information, etc. + Maintains study ... status updates on a weekly basis (eg, IRB approvals, regulatory document collection, patient enrollment, monitoring status, etc.) or as defined by project team +… more
    Sumitomo Pharma (11/21/24)
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