EVMS
Clinical Research Coordinator
Norfolk, VA, US
Sponsorship not specifiedDetected 730 days ago
LogisticsClinical TrialsClinical ResearchResearchCommunicationOrganizational Skills
About the role
- Overview The primary responsibility of the Clinical Research Coordinator is to coordinate the day-to-day administrative and operational logistics of assigned clinical trials.
- As the primary resource for the protocols, the Clinical Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor.
- Along with the investigator, the Clinical Research Coordinator will screen, enroll and follow study subjects, ensuring protocol compliance and close monitoring while the subjects are on study.
Requirements
- Ability to think and work independently, insight, excellent organizational skills, astute and accurate patient assessment skills, and the ability to identify and assign priorities.
- The Clinical Research Coordinator is required to have an in-depth knowledge of protocol requirements and good clinical practices as set forth by federal regulations.
- Experience with phlebotomy and processing/shipping of specimens highly desired.
Nice to have
- Bachelor's degree in science related field Experience in cognitive impairment/dementia research highly desired.
Skills
- Previous experience with clinical research protocols preferred.
Visa & Work Authorization
- As the primary resource for the protocols, the Clinical Research Coordinator will act as liaison between the investigators, primary care providers, the institutional review board (IRB), and the sponsor.
This listing is sourced directly from EVMS's careers page and normalized into a canonical job model.