Regulatory Affairs Specialist

Job Description We’re looking for a highly organized and detail-driven Regulatory Affairs Specialist to join our growing clinical research team in Miami. This role is ideal for someone experienced in managing regulatory submissions, maintaining inspection-ready study files, and supporting fast-paced clinical trial operations across multiple sites. What You’ll Do Manage IRB submissions, amendments, and regulatory documentation Maintain accurate and audit-ready regulatory files (TMF/eTMF) Ensure …