- University of Utah (Salt Lake City, UT)
- …related work experience) required. IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire, and ... **Open Date** 09/26/2025 **Requisition Number** PRN43202B **Job Title** PS Study Coordinator **Working Title** PS Study Coordinator **Career Progression Track**… more
- University of Utah (Salt Lake City, UT)
- …related work experience) required. IRB CITI Course in the Protection of Human Research subjects certificate obtained within six months of hire, and ... **Open Date** 08/28/2025 **Requisition Number** PRN42975B **Job Title** PS Study Coordinator **Working Title** Study Coordinator **Career Progression Track** D… more
- Georgetown Univerisity (Washington, DC)
- …clinical research team. + Act as a liaison with hospital staff, physicians, IRB , review committees, clinical research finance team, and auditors. + Other ... in the world. Requirements Job Overview Serves as clinical research coordinator for phase I, II, and...and obtain and document informed consent according to protocol, institutional policies, and regulatory guidelines for minimal risk studies.… more
- Georgetown Univerisity (Washington, DC)
- …dedication to making a difference in the world. Requirements Job Overview The Clinical Research Coordinator supports the research efforts of Dr. Virginia ... The candidate will work closely with Dr. Steen's clinical research manager, and Dr. Steen and will act as...industry sponsors, and monitors + Submit study protocol for IRB and contract approval. + Recruit patients, consent patients… more
- Beth Israel Lahey Health (Boston, MA)
- **Overview** The purpose of the **Clinical Research Coordinator I** is to coordinate clinical research activities for the Joslin 50-year Medalist Study, ... the Medalist Program. + Identify eligible participants + Inform patients of research and eligibility + Recruiting and scheduling study participants + Assess… more
- University of Rochester (Rochester, NY)
- …data analysis software required Required **LICENSES AND CERTIFICATIONS** + Professional Research Coordinator Certification (SoCRA or ACRP) Preferred The ... role in monitoring, record-keeping and coordinating all phases of human subject research studies to ensure that...Helps recruit and enrolls participants when needed. + Spearheads IRB protocol submissions and amendments, overseeing research … more
- Emory Healthcare/Emory University (Atlanta, GA)
- …can contribute to the excellence of our academic community. **Description** The Research Project Coordinator is responsible for supporting multi-site clinical ... biology, or a related discipline. + Minimum two years of experience coordinating human subjects research , preferably involving individuals with Down syndrome or… more
- University of Maryland, Baltimore (Baltimore, MD)
- …contributes to the conduct of research . * Coordinates the preparation of Institutional Review Board ( IRB ) and Health Insurance Portability ... * Serves as liaison to other departments such as IRB or CCT, outside organizations, government agencies, and product...work as part of a team. * Knowledge of human subjects research , the regulations and policies… more
- Banner Health (Sun City, AZ)
- …interactions with research staff, internal and external investigators, study sponsors and Institutional Review Board ( IRB ). 8. Participates in the ... Master's Degree or advanced certificate degrees preferred. Possession of Clinical Research Coordinator Certification (CRCC). Regulatory knowledge regarding the… more
- Dana-Farber Cancer Institute (Brookline, MA)
- …agencies, and other research organizations. Works interactively with the Office for Human Research Studies (OHRS), Office of Data Quality (ODQ) and the ... Clinical Trials Offices at the various DF/HCC institutions. The Institutional IND Regulatory Coordinator works directly for...continuing reviews, and informed consent documents for SRC and IRB review and approval. + Prepares and… more