Global Regulatory Lead, Gene Therapy Programs

Arbor Biotechnologies in Cambridge, MA is seeking a Director of Regulatory Affairs to lead regulatory strategy and execution across our preclinical and early clinical programs. Reporting to the Chief Medical Officer, you will serve as the Global Regulatory Lead on program teams and as the primary regulatory contact with the FDA and other health authorities.

You will translate strategy into regulatory submissions, briefing materials, and agency interactions, collaborating with internal experts,