Grant Funded Department of Medicine Clinical Research Unit - Clinical Research Coordinator I
Core
Administrative coordination of clinical research studies including recruitment, consent, data collection, and regulatory compliance.
Role type
Clinical Research Coordinator I
Builds
Clinical research studies (industry sponsored, grant funded, or internally funded)
Domain
Healthcare / Clinical Research
Deliverable
client delivery
Required skills
Recruitment and screening, informed consent, data collection, regulatory compliance, adverse event reporting, database management, specimen processing, phlebotomy
Preferred skills
Healthcare experience, medical/pharmaceutical terminology knowledge
Technologies
Databases, word processing, spreadsheets
Responsibilities
Recruit, screen, and enroll eligible study participants; Obtain informed consent from study participants; Collect data from patient charts, medical records, interviews, questionnaires, and diagnostic tests; Collect, process, and ship research specimens; Track and report adverse events and protocol deviations; Coordinate site monitoring or auditing visits; Prepare and submit IRB, R&D, FDA, and funding documents.
Seniority
Individual Contributor, entry-to-mid level