- Stony Brook University (Stony Brook, NY)
- …discussing study protocol. + Documenting research encounters. + Communicating with the Institutional Revenue Board ( IRB ) and the study team. + Other ... Coordinator (PET) **Required Qualifications (as evidenced by an...to cover all shifts. The RSS will work with human research participants with major depressive disorder.… more
- University of Rochester (Rochester, NY)
- …degree Required + OR Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program Required + Or equivalent ... compliance, and queries. + Assists with specimen processing and shipping. + Serves as back-up research coordinator in the absence of the HSRC II. Serves as the… more
- University of Utah (Salt Lake City, UT)
- …issues associated with human research protections and compliance for the Institutional Review Board ( IRB ). Provides direct consultation, ... Details **Open Date** 10/24/2025 **Requisition Number** PRN43397B **Job Title** Institutional Review Board Adm **Working...administers comprehensive educational programs pertaining to human research protections and IRB review … more
- HonorHealth (AZ)
- …Summary Coordinates all activities related to the Institutional Review Board and assures compliance with IRB guidelines and FDA regulations. In ... IRB Coordinator facilitates initial and continuing review of research protocols in compliance with...This includes initial determinations regarding expedited, exempt, or full board review , as well as human… more
- University of Rochester (Rochester, NY)
- …interventional activities, to document adverse events and report to senior study staff, PI, Institutional Review Board ( IRB ), Sponsor, and/or any other ... internal equity considerations._ **Responsibilities:** Coordinates the activities associated with human subject research . RESPONSIBILITIES: - Coordinates the… more
- Wayne State University (Detroit, MI)
- …the primary educator and informational resource for the research community, Institutional Review Board members, faculty, and staff responsible for ... locations and times, associated with IRB submissions, review , and approval of human research...Submission Pre-reviews. Conduct investigator training as directed by the Institutional Review Board ( IRB… more
- University of Rochester (Rochester, NY)
- …the individual, and internal equity considerations._ **Responsibilities:** GENERAL SUMMARY The Human Subject Coordinator (HSRC) Trainee will assist with ... the Adolescent Brain and Cognitive Development (ABCD) Study, a federally funded research study in the Cognitive Neurophysiology Lab. General protocol and directions… more
- General Dynamics Information Technology (Portsmouth, VA)
- …Portsmouth (NMCP). The CRC is responsible for providing research coordination support for IRB - and IACUC -approved human and animal research protocols in ... entity may be required for safety reasons. + Coordinate research activities of assigned IRB and IACUC-approved...leadership skills as the coordinator of complex human and animal research protocols. + Maintain… more
- Vitalief (Livingston, NJ)
- …a leading hospital research center in Livingston, NJ, administering and overseeing Institutional Review Board ( IRB ) activities to ensure compliance ... institutional regulations governing human subjects research . This role supports investigators, staff, and IRB... research . This role supports investigators, staff, and IRB members in the preparation, review , and… more
- University of Rochester (Rochester, NY)
- …+ Bachelor's degree or Associate's degree and completion of 6 months in the Human Subject Research Coordinator Trainee Program + Or an equivalent ... of the individual, and internal equity considerations._ **Responsibilities:** GENERAL PURPOSE The Human Subject Research Specialist I (HSRS I) plays a vital… more
- Mount Sinai Health System (New York, NY)
- …in the preparation and submission of grant applications and documents (eg, Institutional Review Board , Grants and Contracts Office). **Qualifications** ... **Job Description** The Clinical Research Coordinator is an entry human subjects...telephone calls. 3. Assists in the collection, analysis and review of experimental data for publication and presentation. 4.… 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 ... and resources, and much more. Posted Job Title Clinical Research Coordinator A/B Job Profile Title Clinical...responsibilities as assigned CRC-A + Prepare and process all Institutional Review Board ( IRB… more
- University of Miami (Miami, FL)
- …a proven experience in managing regulatory documentation and submissions to entities such as the Institutional Review Board ( IRB ) and the Food and Drug ... OBGYN has an exciting opportunity for a full-time Clinical Research Coordinator 3 to work in Miami,...initial study requests, annual reviews and modifications to the Institutional Review Board ( IRB… 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 ... and resources, and much more. Posted Job Title Clinical Research Coordinator A Job Profile Title Clinical...study documents, and collection of clinical data. Assist with Institutional Review Board ( IRB… more
- Stanford University (Stanford, CA)
- …bodies, which include HIPAA and FDA regulations, Institutional Review Board requirements, and Good Clinical Practices. IRB submissions. + 2-4 years ... Clinical Research Coordinator 2 **School of Medicine,...provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, 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 ... World Report. **Do you have a passion for helping human kind?** The Clinical Research Coordinator...including the Food and Drug Administration (FDA and local Institutional Review Board . **Primary Duties… more
- Mount Sinai Health System (New York, NY)
- …organizes study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). We are ... **Job Description** The Clinical Research Coordinator assists in the daily...well as part of a team. + Familiarity with IRB processes, research ethics, and HIPAA compliance… more
- University of Washington (Seattle, WA)
- …procedures, recruitment, monitoring study progress, data analysis, and work with the UW institutional review board . Current projects include an NIH-funded ... Diseases_** **has an outstanding opportunity open for a** **_Temporary_** ** Research Coordinator .** The Research ...* Research specific training in Protection of Human Research Subjects. * Self-starter and able… more
- Mount Sinai Health System (New York, NY)
- …study information. Assists in preparing grant applications and documents (for eg, Institutional Review Board , Grants and Contracts Office). ... **Job Description** The Clinical Research Coordinator assists in the daily...research experience Non-Bargaining Unit, 857 - Rehabilitation and Human Performance - ISM, Icahn School of Medicine, Rehab… more
- Loyola University Chicago (Chicago, IL)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. * Assemble ... Clinical Research Coordinator II Thank you for...complete study documents/case report forms. * Ensure compliance with research protocols, and review and audit case… more
