Global Regulatory Affairs Specialist – IND/CTA Submissions

A biotechnology company is seeking a Regulatory Specialist to manage documentation packages for global submissions. The ideal candidate will have over 6 years of biotech experience, with a strong focus on CMC regulatory processes. Responsibilities include preparing FDA submissions, developing regulatory strategies, and monitoring guidelines. A BA/BS degree is required, and familiarity with gene editing is preferred. The position offers a competitive salary range of $130,000 to $160,000 USD. #J-18808-Ljbffr