This job is closed
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About the position
The position involves managing the progress of assigned studies, which includes tracking regulatory and IRB submissions and approvals, overseeing recruitment and enrollment processes, ensuring completion and submission of Case Report Forms (CRFs), and generating and resolving data queries. Additionally, the role requires organizing the delivery of investigational products, laboratory supplies, CRFs, and study-specific materials to and from clinical sites.
Responsibilities
- Manage the progress of assigned studies by tracking regulatory/IRB submissions and approvals.
- Oversee recruitment and enrollment processes for clinical studies.
- Ensure completion and submission of Case Report Forms (CRFs).
- Generate and resolve data queries related to the studies.
- Organize the delivery of investigational products and laboratory supplies to clinical sites.
- Coordinate the transportation of CRFs and study-specific materials to and from clinical sites.
