Senior Director, Clinical Quality Assurance

Job Description

• Reporting to the Vice President, Clinical Quality Assurance, the Sr. Director, Clinical Quality Assurance will define and support the quality oversight and management of GCP activities internally at QED and externally with service providers. Further, the Sr. Director, Clinical Quality Assurance will identify and coordinate quality projects leading to process improvement and hence an enhanced status of inspection readiness. • The ideal candidate will have experience working in a GCP practice area, preferably in the biotech/pharmaceutical sector.

Qualifications

• Ability to build relationships and work collaboratively with a variety of individuals within the department, company, and vendors • Strong negotiation skills, flexibility, and ability to provide a solution-based approach to emerging challenges • A strong team player with the ability to effectively communicate sound quality advice cross-functionally based on experience, regulations, and business needs • Ability to simultaneously handle multiple project issues while dealing with time demands, incomplete information, or unexpected events • Bachelor's degree in a scientific discipline or equivalent experience • Minimum of 8 years of experience in a GCP practice area; Clinical Quality Assurance or similar role preferred

Benefits

• Patient Days, where we are fortunate to hear directly from individuals living with the conditions we are seeking to impact throughout the year and learn how we can improve our efforts • A culture inspired by our values: put patients first, think independently, be radically transparent, every minute counts, and let the science speak • An unyielding commitment to always putting patients first. Learn more about how we do this here • A de-centralized model that enables our program teams to focus on advancing science and helping patients. Our affiliate structure is designed to eliminate bureaucracy and put decision-making power in the hands of those closest to the science • A place where you own the vision – both for your program and your own career path • A collaborative, fast-paced, data-driven environment where we inspire ourselves and each other to always perform at the top of our game • Access to learning and development resources to help you get in the best professional shape of your life • Robust and market-competitive compensation & benefits package (Base, Performance Bonus, Equity, health, welfare & retirement programs) • Flexible PTO • Rapid career advancement for strong performers • Potential ability to work on multiple BridgeBio Pharma programs across multiple therapeutic areas over time here • Partnerships with leading institutions • Commitment to Diversity, Equity & Inclusion