- Stanford University (Stanford, CA)
- Clinical Research Coordinator Associate **School of Medicine, Stanford, California, United States** Research Post Date Jun 10, 2025 Requisition # 106623 The Clinical ... Research Coordinator Associate is responsible for the overall management and implementation...regulations; advise the IRB of amendment changes to the protocol and complete annual protocol renewals. Recruit,… more
- Cordis (Irvine, CA)
- …that address unmet and critical medical needs. **Responsibilities** The Clinical Research Associate (CRA) reports to the Clinical Monitoring Manager. The CRA is ... complete, and that the trial is conducted in accordance with protocol requirements, laboratory collections, imaging collections, regulatory requirements. The CRA… more
- University of Southern California (Los Angeles, CA)
- …Associate Director, IACUCApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/IACUC-Manager\_REQ20149219/apply) ... Los Angeles, California Position Overview: We are seeking a dedicated full-time Associate Director, IACUC to lead our team supporting animal research. This key… more
- IQVIA (Los Angeles, CA)
- …the study(ies) and reporting study data as required by the study protocol , applicable regulations and guidelines, and sponsor requirements. Essential Functions * ... recruitment plan in line with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines… more
- IQVIA (Carlsbad, CA)
- …the study(ies) and reporting study data as required by the study protocol , applicable regulations and guidelines, and sponsor requirements. Essential Functions * ... recruitment plan in line with project needs to enhance predictability. * Administer protocol and related study training to assigned sites and establish regular lines… more
- University of Southern California (San Diego, CA)
- …AssociateApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/San-Diego-CA/Clinical-Research- Associate \_REQ20160224/apply) Keck School of Medicine San ... that they are conducted, recorded, and reported in accordance with the protocol , Standard Operating Procedures (SOPs), Good Clinical Practice (GCP), and the… more
- Cedars-Sinai (Los Angeles, CA)
- …this phenomenal opportunity! **Dr. Pramod Butte, Ph.D. is looking for a Clinical Research Associate I to join a diverse team!** The primary focus of the Butte ... the Butte Lab, please visit this website . Serving as a Clinical Research Associate at Cedars-Sinai, you will assist in the effort in validating the clinical trial… more
- Cedars-Sinai (Los Angeles, CA)
- **Job Description** The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program Administrator, or Research Nurse to ... the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering… more
- Cedars-Sinai (Los Angeles, CA)
- …required-transportation will be provided for outreach travel. The Clinical Research Associate I works directly with a Clinical Research Coordinator, Research Program ... the study. Evaluates and abstracts research data and ensures compliance with protocol and research objectives. Responsible for completing case report forms, entering… more
- Cedars-Sinai (Los Angeles, CA)
- …please visit: MIRIAD IBD Biobank & Database | Cedars-Sinai. The Clinical Research Associate I works under the direction of a Clinical Research Coordinator, Research ... and maintenance of study supplies and kits. + Ensures compliance with protocol and overall clinical research objectives. Ensures compliance with all federal and… more