Medical Director, Clinical Development

Join our team in a dynamic hybrid role, offering flexibility to work remotely and from our headquarters in Watertown, MA.

Disc Medicine is a clinical-stage biopharmaceutical company committed to discovering, developing, and commercializing novel treatments for patients who suffer from serious hematologic diseases. We are building a portfolio of innovative, first-in-class therapeutic candidates that aim to address a wide spectrum of hematologic diseases by targeting fundamental biological pathways of red blood cell biology, specifically heme biosynthesis and iron homeostasis. Disc Medicine values collaboration, professional development, and scientific integrity and promotes an inclusive company culture that empowers and inspires.

The Medical Director, Clinical Development is a key clinical leader responsible for providing medical and scientific leadership across the design, execution, and interpretation of clinical development programs supporting Disc’s pipeline. Reporting to the Executive/Senior Medical Director of the program, this individual will be able to work in a fast-paced environment and collaborate with cross-functional teams and external stakeholders to advance innovative therapies from early clinical development through later-stage development and regulatory evaluation.

The Medical Director will be responsible for assigned clinical studies and serve as a key medical interface with Clinical Science, Clinical Operations, Regulatory Affairs, Biostatistics, Pharmacovigilance, CMC, Translational Medicine, Medical Affairs, and other functions. Responsibilities include medical oversight of clinical trials, clinical development strategy and study design, interpretation of emerging data, and support of regulatory and scientific communications.

The initial focus will be a clinical-stage program targeting iron metabolism. The successful candidate will bring expertise in hematology and/or anemia, clinical research experience, and a strong understanding of drug development.

• Provide medical and strategic leadership for assigned programs and studies.
• Partner with the Program Medical Director and cross-functional teams to develop and execute clinical development plans, including objectives, designs, endpoints, milestones, and strategies.
• Provide medical/scientific input into protocols, investigator brochures, informed consents, statistical analysis plans, clinical study reports, and regulatory documents.
• Serve as a subject matter expert on disease biology, clinical practice, treatment paradigms, unmet needs, and the competitive landscape.
• Interpret internal and external data to inform development strategy and program decisions.
• Develop relationships with investigators, KOLs, and external experts and support scientific conferences and competitive intelligence activities.

• Serve as Study Physician and/or Medical Monitor for assigned trials, providing medical oversight of patient safety, data quality, and clinical conduct.
• Contribute to trial design, including patient populations, eligibility criteria, endpoints, assessments, and monitoring strategies.
• Review patient eligibility, protocol deviations, adverse events, laboratory findings, and emerging safety and efficacy data.
• Partner with Clinical Operations, Data Management, investigators, sites, and vendors to support high-quality study execution.
• Support investigator meetings, advisory boards, DSMC meetings, and other clinical/scientific activities.

• Support clinical content for INDs, CTAs, protocols, investigator brochures, annual reports, clinical study reports, and other regulatory submissions.
• Contribute to regulatory strategy and health authority interactions, including preparation for meetings and responses to questions.
• Ensure clinical activities comply with applicable regulations, ICH-GCP, ethical standards, and company SOPs.
• Maintain high standards of scientific rigor, patient safety, data integrity, and compliance.

• Represent Clinical Development on cross-functional program teams and governance forums.
• Collaborate with Clinical Science, Clinical Operations, Regulatory Affairs, Biostatistics, Data Management, Pharmacovigilance, Translational Medicine, CMC, and Medical Affairs.
• Translate clinical/scientific insights into actionable strategies and align…