About this role
Regulatory Associate at K2 Medical Research. Location: Maitland, Florida, United States. Role: Prepare regulatory documents, Maintain audit-ready files, Report deviations to IRB Requirements: Regulatory Associate to develop and maintain regulatory documents for clinical trials, manage start-up/submission activities, and interface with IRB and sponsor. Category: Research and Development (R&D) Seniority: Mid Level Tools: Microsoft Office, Outlook, IRB portals Certifications: certified clinical research professional (ccrp) Commitment: Full Time Workplace: Onsite Languages: English