
Senior Director, GCP Quality & Compliance
Stoke Therapeutics, Bedford, MA, United States
A leading biotechnology company in Massachusetts is seeking a Sr. Director, Clinical Quality Compliance. This role involves overseeing GCP and GCLP compliance for clinical trials, ensuring readiness for inspections, and leading quality management strategies. The ideal candidate has over 15 years of experience in the biotech field, strong knowledge of regulatory guidelines, and is adept at fostering cross-functional collaboration. The position offers a competitive salary, annual bonus, and comprehensive benefits package.
#J-18808-Ljbffr
#J-18808-Ljbffr