About this role
Senior Manager, Regulatory Affairs at Kymera Therapeutics. Location: Watertown, Massachusetts, United States. Role: leading submissions, advising teams, managing interactions Requirements: 5+ years regulatory affairs drug development experience managing INDs/CTAs and designation requests; experience with EU CTR/CTIS; Bachelor’s degree in a scientific discipline required; strong regulatory writing, communication and cross-functional collaboration skills. Category: Legal and Compliance Seniority: Senior Level Tools: Clinical Trials Information System (CTIS), EU Clinical Trials Regulation (EU CTR) Commitment: Full Time Workplace: Onsite Languages: Sundanese, English