About this role
REGULATORY ASSOCIATE at K2 Medical Research. Location: Lady Lake or The Villages. Role: Prepare regulatory documents, Maintain audit-ready files, Report deviations to IRB Requirements: Regulatory Associate with 2+ years clinical research or regulatory experience; CCRP preferred; Bachelor's degree. Category: Legal and Compliance Seniority: Mid Level Tools: MS Office, Outlook, IRB portals, Regulatory documentation tools Certifications: ccrp (certified clinical research professional) Commitment: Full Time Workplace: Onsite Languages: English