Tanner Clinic has an immediate opening for a Clinical Research Coordinator I. The role involves recruitment and coordination of trial subjects, ensuring informed consent, screening subjects through inclusion and exclusion criteria, and adhering to safety and compliance issues. The coordinator will manage the clinical trial, generate source documents on Microsoft Word, coordinate visits, dispense products, manage monitoring visits, and communicate with sponsors and authorities. Responsibilities also include data collection and management, obtaining medical histories and vital signs, performing phlebotomy, lab processing and shipping, recording and managing adverse events, completing case report forms, filing and archiving, and resolving queries. Other duties may be assigned as needed.
Stand Out From the Crowd
Upload your resume and get instant feedback on how well it matches this job.
Industry
Ambulatory Health Care Services
Education Level
No Education Listed
Number of Employees
251-500 employees