Senior Medical Director (Neuromuscular)

Senior Medical Director (Neuromuscular) || Job DescriptionSoufflé TherapeuticsSoufflé Therapeutics is a biotech company focusing on the cell-type specific delivery of genetic medicines. Our team is making a mark in delivery of oligonucleotides to extrahepatic tissues. We thrive in a purpose-built lab and office space in Watertown. Come and join us in our quest!Position SummaryThe Senior Medical Director will lead the clinical strategy and study execution of one of our neuromuscular disease development programs. Working closely with internal and external stakeholders, this individual will drive clinical development plans, provide medical leadership for one or more clinical studies, and contribute to study design, protocol development, safety reviews, data interpretation, regulatory submissions, publications, and presentations. As a key member of the development team, this individual will guide cross-functional activities to achieve program objectives while ensuring compliance with ICH-GCP and applicable regulatory requirements. This is an individual-contributor role with no direct reports at this time.Key ResponsibilitiesClinical Strategy & LeadershipDevelop and execute a multi-year neuromuscular clinical development strategy for one of our clinical programs.Lead creation and execution of medical plans across the US, Europe, and other potential jurisdictions.Provide medical leadership and scientific guidance to a cross-functional program team through all phases of clinical development.Evaluate and integrate emerging scientific, clinical, and competitive insights into development strategies.Clinical Trial Design & ExecutionDrive the development of clinical content including protocols, amendments, investigator brochures, informed consent forms, clinical study reports, statistical analysis plans, and study manuals.Responsible for developing and implementing study protocols in conjunction with the clinical development team.Serve as Medical Monitor, or provide oversight and guidance to designated Medical Monitors, across clinical programs; provide medical oversight, review safety data, and ensure adherence to protocol and regulatory standards.Partner with clinical operations to support site selection, investigator training, and issue resolution during study conduct.Safety & ComplianceOversee the assessment and interpretation of safety data, including adverse events, safety signals, and risk mitigation strategies.Work closely with pharmacovigilance to ensure timely evaluation and reporting of safety information.Ensure clinical programs follow ICH-GCP, ethical standards, and regional/global regulatory requirements.Regulatory & Scientific CommunicationContribute to the preparation and review of regulatory submissions including INDs, CTAs, briefing documents, and NDAs/BLAs.Represent the clinical program in interactions with health authorities such as FDA, EMA, and other global agencies.Develop and review key clinical documents including protocols, investigator brochures (IBs), clinical study reports (CSRs), and publications.Cross-Functional CollaborationPartner cross-functionally with R&D, clinical operations, biostatistics, regulatory affairs, safety, patient affairs, medical affairs, and commercial teams.Provide medical and scientific expertise for internal decision-making and external communication.Support advisory boards, KOL engagement, and scientific congress activities.External EngagementBuild and maintain relationships with investigators, key opinion leaders, and external experts.Stay current on scientific advances, competitive intelligence, and therapeutic area trends to inform program direction.QualificationsM.D. or D.O. required; significant neuromuscular disease clinical development experience strongly preferred (e.g., neuromuscular neurology, physiatry, or related specialty training).Minimum of 8-10 relevant experience with a demonstrated track record of success in clinical research and drug development within academia, biotechnology, and/or the pharmaceutical industry.Demonstrated experience designing and executing clinical programs across multiple phases and geographic regions.Experience with phase 1-3 clinical studies is requiredStrong knowledge of GCP, ICH guidelines, global regulatory requirements, and the drug development process.Proven medical and scientific leadership of cross-functional teams, with experience engaging regulatory agencies, investigators, KOLs, and external partners.Excellent analytical, strategic, and communication skills.Experience authoring and reviewing key clinical and regulatory documents and contributing to global regulatory submissions and health authority interactions.EducationM.D. or D.O. required.Additional Information

Location: This role is based in our Watertown, MA office, requiring 2-3 days on-site per week.

During the first 3 months, on-site presence will be 4-5 days per week to support onboarding.At Soufflé Therapeutics, we are intentional about building an equitable culture. How we treat our people is reflective of this focus. We are an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees.