About this role
AD/ Director, Clinical Regulatory Affairs Gene Therapy at Ocugen OpCo Inc. Location: Malvern, Pennsylvania, United States. Role: Support development, Lead submissions, Engage agencies Requirements: Bachelor’s or Master’s in life sciences; 8+ years regulatory affairs in biotech/pharma with gene therapy; FDA interactions; INDs/CTAs/BLAs; cross-functional collaboration. Category: Research and Development (R&D) Seniority: Senior Level Commitment: Full Time Workplace: Onsite Languages: English