Clinical Trials Coordinator II
About The Position
Under general supervision, coordinates clinical research protocols; interacts with sponsors, investigators, data coordinating centers, and core laboratory personnel as needed; ensures that the regulatory binders are complete and up-to-date; executes and adheres to the clinical trial research protocols; performs follow-up procedures and completes case report forms; prepares documents for IRB submission in compliance with all local, state, and federal regulations. Screens potential research patients for clinical research protocols and gathers data while maintaining patient confidentiality. Navigate patients through clinical trials.
Responsibilities
- Coordinates clinical research protocols
- Interacts with sponsors, investigators, data coordinating centers, and core laboratory personnel as needed
- Ensures that the regulatory binders are complete and up-to-date
- Executes and adheres to the clinical trial research protocols
- Performs follow-up procedures and completes case report forms
- Prepares documents for IRB submission in compliance with all local, state, and federal regulations
- Screens potential research patients for clinical research protocols and gathers data while maintaining patient confidentiality
- Navigate patients through clinical trials
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What This Job Offers
Job Type
Full-time
Education Level
No Education Listed
Number of Employees
5,001-10,000 employees
