Clinical Trials Regulatory Coordinator
Virtua
Virtua is seeking a Regulatory Coordinator to coordinate regulatory activities for phase II-IV clinical trials. The role involves preparing and submitting IRB documents, maintaining study files, and ensuring compliance across central and external IRBs. Local onsite work requires proximity to Marlton, NJ, with collaboration across the clinical research team. Responsibilities include preparing renewals, amendments, adverse event reporting, and maintaining communications with investigators and IRB #J-18808-Ljbffr Virtua
Vacancy posted 5 days ago
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