- Beth Israel Lahey Health (Burlington, MA)
- …in accordance with Research SOPs, FDA , OHRP, and GCP regulations . + Immediately develops coordinator /sponsor relationship. + Completes start-up checklists ... more
- University of Utah (Salt Lake City, UT)
- …team member. * Possess knowledge of all ULEB procedures, EBAA Medical Standards, and FDA regulations pertaining to eye banking. * Know and follow current ... more
- University of Southern California (Los Angeles, CA)
- …(IRB, FDA , etc) to ensure compliance with local, state, and national regulations . This research coordinator will report to the Principal Investigator and ... more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator - A/B (Department of Translational Medicine and Human Genetics) Job Profile ... more
- WMCHealth (Valhalla, NY)
- …all aspects of study progress from start-up to close-out activities in accordance with FDA , GCP, ICH guidelines, local regulations and corporate policies. + Work ... more
- University of Colorado (Aurora, CO)
- …educate and train staff on compliance with all standards. + Assess updates to FDA regulations on human cells, tissues, and cellular and tissue-based products ... more
- University of Colorado (Aurora, CO)
- **Clinical Research Coordinator (Open Rank) Lung Team** **Description** **University of Colorado Anschutz Medical Campus** **Department: Cancer Center** **Working ... more
- University of Utah (Salt Lake City, UT)
- …maintains study records, materials, and databases to ensure compliance with study protocols, FDA , IRB , departmental, and university regulations . + Prepares ... more
- Dana-Farber Cancer Institute (Boston, MA)
- …Prepares and submits regulatory documentation that may include; IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate ... more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C (Abramson Cancer Center) Job Profile Title Clinical Research Coordinator ... more
- University of Utah (Salt Lake City, UT)
- …**Dept. Preferences** Previous clinical research experience. Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations ; an understanding of research ... more
- University of Utah (Salt Lake City, UT)
- …within six months. **Preferences** **Department Preferences** + Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations . + An understanding of ... more
- University of Pennsylvania (Philadelphia, PA)
- …wellness programs and resources, and much more. Posted Job Title Clinical Research Coordinator B/C Job Profile Title Clinical Research Coordinator B Job ... more
- University of Utah (Salt Lake City, UT)
- …relations and effective communication skills also required. Knowledge of Good Clinical Practices, FDA , HIPAA and IRB regulations ; an understanding of research ... more
- Dana-Farber Cancer Institute (Boston, MA)
- …Prepares and submits regulatory documentation that may include; IND/IDE applications, FDA annual reports, Serious Adverse Event reports, to the appropriate ... more
- University of Pennsylvania (Philadelphia, PA)
- …programs and resources, and much more. Posted Job Title Clinical Research Coordinator C (Hybrid Eligible) Job Profile Title Clinical Research Coordinator ... more
- UCLA Health (Los Angeles, CA)
- …The Department of Surgery is seeking to hire a full time Regulatory Coordinator to coordinate and participate in all regulatory research activities. In this role ... more
- AdventHealth (Orlando, FL)
- …trials in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices ... more
- University of Southern California (Los Angeles, CA)
- …Coordinator IApply (https://usc.wd5.myworkdayjobs.com/ExternalUSCCareers/job/Los-Angeles-CA Health-Sciences-Campus/Research- Coordinator -I\_REQ20157582-1/apply) ... more
- AdventHealth (Orlando, FL)
- …trials in accordance with trial protocols, Food and Drug Administration ( FDA ) regulations and International Conference on Harmonization/Good Clinical Practices ... more