- University of Miami (Miami, FL)
- …to protocol requirements, UM and department policy. + Distributes study drug materials according to practice standards and clinical credentials as delegated ... by the Principal Investigator . + Monitors, documents, reports, and follows-up on study...staff. + Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports… more
- University of Miami (Miami, FL)
- …according to protocol requirements, UM and department policy. Distributes study drug materials according to practice standards and clinical credentials as delegated ... by the Principal Investigator . + Monitors, documents, reports, and follows-up on study...staff. + Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports… more
- University of Miami (Miami, FL)
- …according to protocol requirements, UM and department policy. 5. Distributes study drug materials acco rding to practice standards and clinical credentials as ... delegated by the Principal Investigator . 6. Monitors, documents, reports, and follows - up...staff. 9. Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports… more
- HCA Healthcare (Overland Park, KS)
- …The **Clinical Research Coordinator (CRC)** assists the principal investigator (PI) and sub investigators with all ... cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free...+ Coordinates all research study activities with the Principal Investigator and has no direct nursing care responsibilities. +… more
- University of Miami (Miami, FL)
- …according to protocol requirements, UM and department policy.5. Distributes study drug materials according to practice standards and clinical credentials as ... delegated bythe Principal Investigator .6. Monitors, documents, reports, and follows-up on study unanticipated/adverse events and protocoldeviations.7. Assists in… more
- ThermoFisher Scientific (Wilmington, NC)
- …knowledge and experience working on clinical trials through every stage of drug development. This includes management and oversight of all contracted services. ... practice, and regulatory requirements are followed. Attends and presents at investigator and sponsor meetings, provides medical consultation to clients, … more
- Bozeman Health (Bozeman, MT)
- …trials in accordance with Good Clinical Practice (GCP) under the direction of investigators and the director. The CRC ensures adherence to research standards set ... forth by the Food and Drug Administration (FDA), Office for Human Research Protections (OHRP),...+ Complete and maintain required regulatory documentation in the Investigator Site File and sponsor-provided/departmental vendor systems. + Manage… more
- Sanofi Group (Morristown, NJ)
- …ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could ... abstracts and/or manuscripts; clinical pharmacology or ECET components of investigator brochures, regulatory documents. + Interact effectively with managers from… more
- University of Miami (Miami, FL)
- …to protocol requirements, UM and department policy. + Distributes study drug materials according to practice standards and clinical credentials as delegated ... by the Principal Investigator . + Monitors, documents, reports, and follows-up on study...staff. + Monitors protocol implementation and study progress; keeps investigators fully apprised of study progress; submits progress reports… more
- HCA Healthcare (Richmond, VA)
- …common services at no cost or for a low copay. Plans include prescription drug and behavioral health coverage as well as free telemedicine services and free AirMed ... multiple research protocols and serving as a liaison with local investigators , clinical staff, and research personnel. Under direct supervision, this individual… more