Associate Director, GCP Quality

Kymera Therapeutics is seeking an Associate Director, GCP Quality to develop, implement, and maintain the Good Clinical Practice (GCP) Quality framework to support global clinical development programs. The role will provide independent quality oversight of clinical trials, CROs, and vendors to ensure compliance with ICH GCP, global regulatory requirements, and internal quality standards.

Requirements

• Bachelor's degree in life sciences or related field required
• 8+ years of experience in GCP Quality, Clinical QA, or Clinical Operations with strong QA focus in a sponsor organization
• Experience supporting regulatory inspections is a plus
• Deep knowledge of ICH GCP (E6 R2/R3)
• Experience with risk-based monitoring and RBQM frameworks, TMF systems and electronic platforms
• Working knowledge of global regulatory requirements and strong understanding of data integrity principles

Benefits

• Competitive compensation package
• Annual bonus
• Equity participation
• Comprehensive benefits