About this role
Regulatory Coordinator II - Clinical Trial Office at Danafarber. Location: Brookline or Maine or Vermont or New Hampshire or Massachusetts or Connecticut or Rhode Island. Role: preparing submissions, maintaining records, coordinating start-up Requirements: Completes regulatory submissions and tracking for clinical trials (IND/IDE, IRB, FDA), maintains regulatory files, coordinates study start-up, and ensures compliance with FDA and ICH/GCP; requires bachelor’s degree or equivalent experience and 1–3 years regulatory experience. Category: Research and Development (R&D) Seniority: Entry Level Tools: Microsoft applications, databases Commitment: Full Time Workplace: Hybrid Languages: English