- Rush University Medical Center (Chicago, IL)
- …(CCRP), Certified Clinical Research Associate (CCRA), Certified Clinical Research Coordinator (CCRC), or Certified IRB Professional (CIP) strongly ... continuing review applications and unanticipated problems. * Communicates with IRB and finalizes documents based on IRB comments and recommendations… more
- University of Miami (Miami, FL)
- …studies. + Develop, review and submit required documentation to the UM/JMH IRB to ensure successful approval of research protocols. Maintain any reports and ... 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) . Clinical Research… more
- Mount Sinai Health System (New York, NY)
- …and training to multiple study teams who develop and submit documentation and information for Institutional Review Board ( IRB ) review and who ... revises regulatory standard operating policies and procedures. + Submits protocol applications for IRB review in a timely manner; tracks new protocols through… more
- University of Utah (Salt Lake City, UT)
- …and strict protocol implementation/adherence; oversee compliance with GCP guidelines, federal regulations, institutional policies and procedures, and internal ... Rate Range** $22.88 to $40.50 **Close Date** 10/31/2025 **Priority Review Date (Note - Posting may close at any...Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations; an understanding of research procedures;… more
- University of Pennsylvania (Philadelphia, PA)
- …duties such as preparation and submission of regulatory documents through the IRB (initial submissions, amendments, and continuations). The research coordinator ... duties such as preparation and submission of regulatory documents through the IRB (initial submissions, amendments, and continuations). The research coordinator… more
- Emory Healthcare/Emory University (Atlanta, GA)
- …gathers accurate information to develop various publications. + Acts as liaison to the Emory Institutional Review Board ( IRB ) and other ethical review ... committees in preparation, submission, and maintaining IRB clearance for research , surveys, and other studies conducted by the program. Updates IRB … more
- Cedars-Sinai (Los Angeles, CA)
- …local agency requirements including the Food and Drug Administration (FDA) and local Institutional Review Board . **Primary Job Duties and Responsibilities:** ... **Job Description** **Innovative care begins with research !** We invite you to consider this phenomenal...works with Principal Investigator (PI) to complete and submit federal and non- federal grants and serves… more
- University of Utah (Salt Lake City, UT)
- …the study. 6. Represents the research program at meetings, national and international research consortia. 7. Prepares, submits and maintains IRB , FDA , NCI ... Rate Range** 39300 to 61384.25 **Close Date** 01/23/2026 **Priority Review Date (Note - Posting may close at any...Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations; an understanding of research procedures;… more
- Dana-Farber Cancer Institute (Boston, MA)
- …entities as required. Maintains regulatory binders and ensures study compliance with all state, federal , and IRB requirements. May be responsible for IRB ... The Gastrointestinal (GI) Oncology Clinical Research Program at Dana-Farber Cancer Institute is seeking...start-up process from receipt of protocols through the Scientific Review Committee and IRB submissions, and site… more
- University of Colorado (Aurora, CO)
- … research subsites. + Coordinate, delegate, and update tasks related to research studies and programs, including grant preparation, IRB documents, and study ... to maintain and enhance relationships. + Manage all necessary documentation for research activities, including IRB applications, recruitment, consent forms, and… more