Clinical Trials Regulatory Specialist
Actalent
Actalent is seeking a Regulatory Specialist to manage regulatory files for assigned clinical trials, prepare submissions to IRBs, sponsors, and CROs, and ensure compliance with FDA/ICH-GCP guidelines. The role requires at least 2 years of regulatory experience, strong attention to detail, and the ability to work independently with cross-functional teams. This is a fully onsite contract-to-hire position in Miami, FL with hourly compensation. #J-18808-Ljbffr Actalent
Vacancy posted 2 days ago
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