Senior Medical Director, Clinical Development

Editas Medicine•Cambridge, MA

2d•$345,000 - $375,000

About The Position

At Editas Medicine, we are pioneering the possible. Our mission and commitment is to translate the power and potential of the CRISPR/Cas12a and CRISPR/Cas9 genome editing systems into a robust pipeline of medicines for people living with serious diseases around the world. Our goal is to discover, develop, manufacture, and commercialize transformative, durable, precision genomic medicines for a broad class of diseases. At Editas Medicine, we’re a team of passionate problem solvers, harnessing the power and potential of CRISPR gene editing to transform the future of medicine. Driven by a shared purpose to serve people living with serious diseases, we succeed together through collaboration, mutual respect, and innovation. If you want to be part of a team where your voice is heard and respected, where you can operate at the forefront of gene editing, and push the boundaries of what’s possible in medicine, come join us and become an Editor! The Senior Medical Director, Clinical Development will provide medical, scientific, and operational leadership for clinical programs focused on genetic diseases and gene-editing therapeutics, with an emphasis on early-stage and proof-of-concept studies. Reporting to the Chief Medical Officer, this physician-scientist will lead the design, execution, and optimization of global clinical trials, including the establishment and oversight of sponsor-led studies and the management of key academic and operational partnerships. With EDIT-401 approaching clinical development and a rapidly advancing pipeline, this role offers the opportunity to shape both current programs and future portfolio strategy while serving as a close partner to the research organization and CMO. Ideal candidates will thrive in a fast-paced biotech environment, combining scientific expertise, strategic thinking, and hands-on clinical execution to drive successful program outcomes.

Requirements

MD or MD/PhD with training in cardiovascular diseases, internal medicine, rare disease, or related fields.
10+ years of industry experience in clinical research and development, including leadership of early-stage cardiovascular disease and/or rare disease programs.
Demonstrated experience designing and executing global clinical trials; experience with gene-editing, gene therapy, or advanced modalities is a plus.
Hands-on experience establishing or overseeing clinical trials, including collaboration with local CROs, investigators, and hospital partners.
Willingness to travel to develop and oversee global clinical trials.
Strong understanding of clinical trial methodology, translational science, safety monitoring, and global regulatory pathways.
Proven ability to work effectively in matrixed teams and influence across scientific, operational, and business stakeholders.
Exceptional written and verbal communication skills, including experience presenting to investigators, regulators, and internal governance bodies.
Strategic, pragmatic, and able to thrive in a high-growth, mission-driven biotech environment.
Strong network of clinical investigators and scientific collaborators globally, enabling effective partnership-building, and study execution.

Nice To Haves

experience with gene-editing, gene therapy, or advanced modalities is a plus.

Responsibilities

Lead the design, medical oversight, and operational execution of clinical development strategies for EDIT-401, with emphasis on early development (FIH, Phase 1–2) and translational endpoints relevant to gene editing.
Serve as clinical program lead, providing day-to-day medical and scientific leadership to ensure high-quality clinical execution and data integrity.
Partner closely with R&D to integrate biomarker strategy, safety monitoring approaches (e.g., immunogenicity, off-target assessments), and indication rationale.
Contribute to the development and refinement of clinical development plans and study protocols, ensuring alignment with global regulatory expectations.
Support preparation of clinical documents for regulatory submissions (IND, CTA, NDA/BLA components, study reports), with specific focus on medical content and scientific rationale.
Collaborate with regulatory affairs and region-specific experts to ensure readiness for interactions with global regulatory agencies.
Work closely with Clinical Operations, Regulatory, Project Management, CMC, Analytical Sciences, and Commercial to ensure integrated planning and execution.
Partner with Research teams on indication selection, biomarker development, and advancing new pipeline programs.
Provide clinical leadership in cross-functional forums, risk assessments, data reviews, and stage-gate processes.
Cultivate strong networks with global investigators, KOLs, and patient advocacy groups.
Lead or support scientific advisory boards, investigator meetings, and data-review interactions.
Represent the company at scientific conferences and contribute to manuscripts, abstracts, and presentations.