This position is responsible for preparing and submitting regulatory submissions to the IRB and sponsors, ensuring documentation compliance for multiple study projects, audit preparation, and data submission. The role involves advising patients on trial design, facilitating informed consent for investigators, strictly adhering to protocol procedures for each study, screening for potential trial patients based on eligibility criteria, and managing patient follow-up. The position is responsible for the coordination of these trial activities, among others.
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Job Type
Full-time
Career Level
Mid Level
Education Level
Associate degree