Clinical Regulatory Specialist - IRB & FDA Submissions
Listed on 2026-10-16
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Healthcare
Healthcare Compliance, Clinical Research
Actalent is seeking a Regulatory Specialist to manage and maintain inspection-ready regulatory files for assigned clinical trials. You will prepare and submit regulatory documents, track deadlines, and ensure adherence to FDA, ICH-GCP, and IRB requirements.
The role requires at least 2 years of regulatory experience in clinical research, strong attention to detail, and proficiency with MS Office. This is a fully onsite, contract-to-hire position based in Miami, FL.
The following opportunity is for a Clinical Regulatory Specialist - IRB & FDA Submissions with Actalent.
Our team is growing, and we are hiring a Clinical Regulatory Specialist - IRB & FDA Submissions in Miami, FL, United States.
This opportunity is for the Clinical Regulatory Specialist - IRB & FDA Submissions role at Actalent.
We are seeking a motivated Clinical Regulatory Specialist - IRB & FDA Submissions to join Actalent in Miami, FL, United States.
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