Regulatory CMC Lead, Gene Therapy — Global Submissions

A genetic medicine company in Boston is seeking an Associate Director of Regulatory CMC to lead regulatory strategy and bridge development with regulatory roles. This hybrid position requires strong regulatory affairs experience in biotechnology, excellent communication skills, and the ability to work collaboratively across teams. The ideal candidate will handle CMC content for clinical trials and engage with agency interactions. The role offers competitive compensation between $170,000 and $220,000 along with extensive benefits. #J-18808-Ljbffr