Medical Director, Clinical Development

Guide Prime Editing programmes from preclinical research into human studies. The medical director develops trial strategies and protocols, monitors participant safety and clinical data, and works with research colleagues on translational biomarkers. Responsibilities also include investigator engagement, regulatory discussions and scientific presentations. The role is based in Cambridge, Massachusetts, with travel of up to 25%.

MD or equivalent, preferably MD-PhD, with at least three years of industry or comparable academic experience in relevant research or clinical trials. Requires knowledge of gene therapy, genetics, immunology and Good Clinical Practice. Pulmonology or hepatology specialisation is preferred.