- Tufts Medicine (Boston, MA)
- …study sponsor and Institutional Review Board . 5. Assists with Institutional Review Board ( IRB ) requirements for each study including meeting ... related activities. 2. IATA Hazardous Good Shipping certification. 3. CITI Human Research Protection certification. **Duties and Responsibilities** **:** The… more
- Dartmouth Health (Lebanon, NH)
- …regulatory agencies. * May maintain study and regulatory documentation including working with the Institutional Review Board ( IRB ), ensuring all staff ... onboards, trains and oversees new clinical research coordinator staff on Good Clinical Practice (GCP), Human...and quality of life issues depending on complexity with review by principal investigator with collection of source data… more
- Kelly Services (Kansas City, MO)
- …activities adhere to ethical and regulatory guidelines, such as Good Clinical Practice GCP and Institutional Review Board IRB protocols. + Reporting: + ... **Clinical Research Data Coordinator ** **Kelly(R) Science &...data, identify discrepancies, and address issues promptly. + Literature Review : + Stay updated on current research … more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions and ensure Institutional Review Board renewals are completed. + Monitor ... Clinical Research Coordinator Associate **School of Medicine,...Experience acquiring and/or preprocessing fMRI data + Knowledge of human subjects research regulations ( IRB ,… more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure Institutional Review Board renewals are completed. + Assemble ... Cancer Clinical Research Coordinator Associate - Hematology (Hybrid)...complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case… more
- Trinity Health (Ann Arbor, MI)
- … Nurses, Sub-Investigators, and Principal Investigator. + Acts as liaison between the Institutional Review Board ( IRB ), Investigator, clinical ... **POSITION PURPOSE** Responsible for coordinating regulatory requirements necessary for oncology research trials associated with the Michigan Cancer Research … more
- Stanford University (Stanford, CA)
- …for completion and accuracy with source documents. Prepare regulatory submissions, and ensure institutional Review Board renewals are completed. + Assemble ... Neuromuscular Clinical Research Coordinator Associate **School of Medicine,...complete study documents/case report forms. + Ensure compliance with research protocols, and review and audit case… more
- Stanford University (Stanford, CA)
- …regulations; provide leadership in identifying and implementing corrective actions/processes. Monitor Institutional Review Board submissions, and respond to ... Clinical Research Coordinator II **School of Medicine,...governing bodies, which include HIPAA and FDA regulations, + Institutional Review Board requirements, and… more
- University of Pennsylvania (Philadelphia, PA)
- …documents through the IRB (initial submissions, amendments, and continuations). The research coordinator should be interested in and capable of developing ... collaborating investigators and CNDS staff in carrying out CNDS research . S/he will be trained to conduct human... IRB (initial submissions, amendments, and continuations). The research coordinator should be interested in and… more
- University of Utah (Salt Lake City, UT)
- Details **Open Date** 10/09/2025 **Requisition Number** PRN16440N **Job Title** Clinical Research Coordinator , Sr. **Working Title** Clinical Research ... Medicine has an immediate opening for a Sr. Clinical Research Coordinator (Sr. CRC ). The Sr....Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations; an understanding of research procedures;… more