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Medical Director/Senior Medical Director, Clinical Development, Genetic Diseases Jobs

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Medical Director/Senior Medical Director, Clinical Development, Genetic Diseases
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Lead clinical development for innovative in-vivo base editing programs targeting genetic metabolic disorders. As Medical Director, you will design trials, provide medical monitoring, and support global regulatory strategy. This Cambridge-based role requires an MD with 15+ years' experience, inclu...
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United States , Cambridge
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Salary
210000.00 - 375000.00 USD / Year
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Beam Therapeutics
Expiration Date
Until further notice
Pursue a career at the forefront of medical innovation by exploring Medical Director and Senior Medical Director jobs in Clinical Development for Genetic Diseases. This high-impact profession sits at the strategic and scientific core of bringing transformative therapies to patients with rare and inherited conditions. Professionals in these roles are physician-scientists who translate groundbreaking genetic science into viable clinical programs, guiding potential treatments from concept through regulatory approval. Typically, a Medical Director in this field serves as the primary medical lead for one or more therapeutic programs. Their central responsibility is to architect and execute the Clinical Development Plan (CDP), which defines the pathway for proving a therapy's safety and efficacy. This involves designing robust clinical trial protocols, determining appropriate patient populations, endpoints, and biomarkers, and ensuring the scientific integrity of every study phase. A critical day-to-day function is medical monitoring, where the director actively reviews patient safety data, assesses efficacy signals, and provides medical guidance to cross-functional study teams to ensure patient safety and protocol adherence. The role is deeply collaborative, requiring leadership within a matrix environment. Medical Directors co-lead clinical sub-teams and work closely with colleagues in regulatory affairs, biometrics, clinical operations, and pharmacology. They are the key scientific voice in interactions with health authorities, contributing to Investigational New Drug (IND) applications, briefing packages, and regulatory responses. Externally, they establish and nurture relationships with key opinion leaders (KOLs), principal investigators, and patient advocacy groups, often leading advisory boards to gain critical insights that shape clinical strategy. Typical requirements for these senior positions include an MD, DO, or equivalent medical degree, often complemented by board certification or significant experience in a relevant specialty like pediatrics, neurology, endocrinology, or genetics. Industry experience within pharmaceutical or biotechnology settings is essential, with a strong preference for backgrounds in clinical development, particularly in rare diseases, gene therapy, or cell therapy. Successful candidates possess a unique blend of deep scientific expertise, strategic vision, and operational acumen. They must have exceptional communication skills to articulate complex data, the leadership ability to influence without direct authority, and the resilience to thrive in a fast-paced environment addressing high-unmet medical needs. For physicians passionate about driving the future of genetic medicine, these jobs offer an unparalleled opportunity to shape the landscape of care for generations to come.

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