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Director, Program Management Full Life Cycle IND to Phase II

Monte Rosa Therapeutics
September 08, 2026
Full-time
Remote friendly (Boston, MA)
Worldwide
Clinical Research and Development
Role: Senior leader in program management overseeing immunology and inflammation assets from IND through Phase 2/3, responsible for strategic and operational planning to ensure successful development and regulatory submission. Responsibilities include developing integrated cross-functional plans, scenario and risk analysis, managing timelines and resources, and facilitating collaboration across clinical, regulatory, CMC, and translational teams. The role emphasizes agility in evolving scientific landscapes, with a focus on resource optimization, risk mitigation, and executive communication. Qualifications: minimum 12+ years in biotech/pharma, with 8+ years leading cross-functional teams in immunology or inflammation drug development; proven experience advancing assets through Phase 2/3, and supporting regulatory meetings; BS required, MS/PhD or MBA preferred; PMP certification desirable. High-Value: expertise in immunology, inflammation, biomarker strategies, and end-to-end drug development in resource-constrained biotech settings; experience with regulatory pathways and clinical phases; leadership in small to mid-sized biotech environments; familiarity with project management tools like Smartsheet or MS Project. Location: Boston, MA. The position demands a strategic, hands-on leader with strong influencing, communication, and organizational skills, capable of navigating ambiguity and fostering cross-functional alignment in a fast-paced, innovative setting.