About this role
(Senior) Manager, Regulatory Affairs at Braveheart Bio. Location: San Francisco, California, United States. Role: managing submissions, coordinating deliverables, managing queries Requirements: Bachelor's degree, 5+ years regulatory affairs experience in biotech/pharma with strong focus on EU and ex‑U.S. clinical trial submissions (CTIS/CTA); experience managing CROs, health authority interactions, and regulatory lifecycle activities. Category: Research and Development (R&D) Seniority: Senior Level Tools: CTIS, Veeva RIM Commitment: Full Time Workplace: Hybrid Languages: tc, English