- University of Colorado (Aurora, CO)
- …+ Assist with and oversee the day-to-day operations of clinical trials and studies + Obtain study subject's medical history and current medication information, ... to protocols, informed consent forms, and all other essential study documents for assigned studies + Independently...delete duties and responsibilities at the discretion of the supervisor and/or hiring authority. - this role is eligible… more
- Bon Secours Mercy Health (Midlothian, VA)
- …Cancer Institute. **Essential Job Functions** : + Enroll patients in research studies , associating visits / appointments / admissions with research studies ... to Insurance and which are billed to the research study . **Project Management** : + Organize and monitor clinical...Organize and monitor clinical research observational and data collection studies . + Serve as Liaison between Bon Secours Cancer… more
- University of Miami (Miami, FL)
- …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Addresses adverse events per protocol, advocating for study … more
- Stanford University (Stanford, CA)
- … studies . Work under close direction of the principal investigator and/or study coordinator/ supervisor . **Duties include:** + Serve as primary contact with ... Coordinator Associate to perform duties related to the coordination of clinical studies in diabetes and immunology. Coordinate moderately complex aspects of one or… more
- Stanford University (Stanford, CA)
- … studies . Work under close direction of the principal investigator and/or study coordinator/ supervisor . At Stanford University School of Medicine, the work we ... Associate (Fixed-term 1 year) to perform duties related to the coordination of clinical studies . Coordinate moderately complex aspects of one or more clinical… more
- Regeneron Pharmaceuticals (Tarrytown, NY)
- …of: - Early clinical strategy in terms of indication selection, study rationale, scientific/clinical endpoints - POC-enabling human studies , First-In-Human ... sector, or academic or clinical setting. You will work closely with supervisor and other members of the cross-functional team, contributes to early development… more
- University of Miami (Boca Raton, FL)
- …procedures according to the protocol. + Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants. + Addresses adverse events per protocol, advocating for study … more
- University of Pennsylvania (Philadelphia, PA)
- …and external groups. Work directly with investigators to design, set-up and execute studies . Accountable for making sure study timelines and goals are met. ... disease states and varying complexities. Research coordinator work includes study design, protocol development, submission to review boards, subject recruitment… more
- University of Miami (Miami, FL)
- …procedures according to the protocol.3. Coordinates routine activities of clinical studies including data collection and maintenance, planning study timelines, ... informing the PI/ supervisor of adverse events, including those reported by study participants.7. Addresses adverse events per protocol, advocating for study … more
- Alaka'ina Foundation Family of Companies (Frederick, MD)
- …Inspector General as required. + Support 1-3 Non-human Primate studies , 40-50 rodent studies per year. Shall coordinate all study activities with study ... as needed. + CONUS/OCONUS travel may be required in support of approved studies and/or presentation of scientific research. + Prepare and participate in BSL-2 and… more