- University of Miami (Miami, FL)
- …Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Clinical Research Coordinator 2 to work at the UHealth Medical Campus in Miami, FL. ... more
- University of Miami (Miami, FL)
- …Department of SCCC has an exciting opportunity for a Full Time Clinical Research Coordinator 2 to work Hybrid at the UHealth Medical campus in Miami, ... more
- University of Miami (Miami, FL)
- …and participant compensation/reimbursement records. + Prepares and submits annual continuing reviews to the Institutional Review Board ( IRB ). + Notifies ... more
- University of Miami (Miami, FL)
- …Miami/UHealth Department of SCCC has an exciting opportunity for a Full Time Clinical Research Coordinator 2 to work in the UHealth Medical campus in Miami, FL. ... more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions and respond to ... more
- University of Miami (Miami, FL)
- …of Miami Health System, "UHealth" has an exciting opportunity for a Full-Time Clinical Research Coordinator 2 to work in the Peggy and Harold Katz Family Drug ... more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... more
- University of Miami (Coral Gables, FL)
- …. The University of Miami/UHealth is currently seeking a full time Clinical Research Coordinator 2 to work in Coral Gables, FL. The Department of Physical ... more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... more
- Methodist Health System (Dallas, TX)
- …team members to provide the very best care for our patients. The Research Coordinator 2 perform coordination of all phases of the research process. The ... more
- Baylor Scott & White Health (Plano, TX)
- …professionals, and working with Pharmacy to ensure a smooth project flow. + Reports to the Institutional Review Board ( IRB ), completing IRB review ... more
- UCLA Health (Los Angeles, CA)
- …+ Background in data management of clinical research protocols preferred + Prior IRB experience and coordination of clinical studies desired + RN licensure a plus ... more
- University of Pennsylvania (Philadelphia, PA)
- …entry, organizing, maintaining, and assuring the accuracy of all study documentation. The coordinator will oversee 2 or more clinical trial ensuring that the ... more
- Actalent (Atlanta, GA)
- …Skills + Good Clinical Practice (GCP) knowledge + Patient consenting + Clinical Research Coordinator (CRC) experience + SAE reporting + 2 + years of solid CRC ... more
- Vitalief (Las Vegas, NV)
- …for database lock. Required Skills: + Bachelor's Degree "OR" Certified Clinical Research Coordinator (SOCRA or ACRP) preferred. + Two ( 2 ) years of experience ... more
- University of Pennsylvania (Philadelphia, PA)
- … B will assist the regulatory specialist in preparing for all local and Central Institutional Review Board ( IRB ) documentation through the IRB ... more
- University of Pennsylvania (Philadelphia, PA)
- …protocols in accordance with Good Clinical Practices, HIPAA, and other federal/ institutional requirements, and ( 2 ) meet required obligations to ... more
- Cedars-Sinai (Beverly Hills, CA)
- …study conduct. Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more
- University of Pennsylvania (Philadelphia, PA)
- …biological samples and related study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB ) filings and inquiries, and ... more
- Cedars-Sinai (Los Angeles, CA)
- …study conduct. + Works closely with a regulatory coordinator or directly with the Institutional Review Board ( IRB ) to submit Adverse Events, Serious ... more