- Monster (Chicago, IL)
- …and completion of submissions, amendments, and adverse event reports as required by the UIC Institutional Review Board ( IRB ), Protocol Review ... (eg phlebotomy, centrifugation, interviewing). Preferred Qualifications Certified Clinical Research Coordinator (CCRC) preferred. Prior experience with medical… 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** 09/04/2025 **Requisition Number** PRN43033B **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
- Trinity Health (Syracuse, NY)
- **Employment Type:** Full time **Shift:** Day Shift **Description:** ** Institutional Review Board Specialist - St. Joseph's and St. Peter's Health Systems** ... Summary** : Responsible for coordinating the operations of SJH/SPHP ( IRB ), the IRB Coordinator is...matters pertaining to protecting the rights and welfare of human research participants. + Ensures that submitted… 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
- 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
- University of Colorado (Aurora, CO)
- …Office of Regulatory Compliance - Colorado Multiple Institutional Review Board ** **Job Title: IRB Panel Coordinator ** **Position #:00696471 - ... Review Boards or OHRP/FDA regulations regarding human subject research + Certified IRB...the Colorado Multiple Institutional Review Board (COMIRB) conducts reviews of submitted human … 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. + Assists in the collection, analysis and review of experimental data for publication and presentation. +… 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
- 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 ... you have a passion for helping humankind?** The Clinical Research Coordinator II works independently, providing study...including the Food and Drug Administration (FDA) and local Institutional Review Board ( IRB… 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
- 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...of a team, as well as independently; knowledge of IRB and human research protection… more
- Nuvance Health (Danbury, CT)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... *Description* *Clinical Research Coordinator - Danbury Hospital* *Full-time,...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… more
- Nuvance Health (Norwalk, CT)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... *Description* *Clinical Research Coordinator - Norwalk, CT* *Full-time:...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… more
- Nuvance Health (Poughkeepsie, NY)
- … patient, protocol implementation, data collection and query resolution, and submission to the Institutional Review Board ( IRB ). Coordinates studies in ... *Description* *Clinical Research Coordinator - Poughkeepsie, NY* *40...protocols, consent forms, and other required documents to the Institutional Review Board ( IRB… 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
- Texas A&M University System (Kingsville, TX)
- …University-Kingsville regulations. This includes providing administrative and regulatory oversight for the Institutional Review Board ( IRB ), ... + Coordinates the review and processing of research protocols for IRB ( human ...institutional policies. Export Control Compliance: + Assists with review of research activities for restrictions, technology… more
- Dartmouth Health (Lebanon, NH)
- …standards operating procedures for the execution of clinical trial operations, including timely Institutional Review Board ( IRB ) submissions meeting ... Overview Clinical Research Coordinator I works closely with...with regulatory processes. * Maintains basic current understanding of IRB and Dartmouth-Hitchcock Health (D-HH) Institutional processes.… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure institutional Review Board renewals are completed. + Assemble ... Clinical Research Coordinator Associate **School of Medicine,...IRB . Protect the rights, safety and well-being of human subjects involved in the clinical trials. **Duties include*:**… more
