Vice President, Global Respiratory Products Leader

About Generate:Biomedicines Generate:Biomedicines is a new kind of therapeutics company – existing at the intersection of machine learning, biological engineering, and medicine – pioneering Generative Biology™ to create breakthrough medicines where novel therapeutics are computationally generated, instead of being discovered. The Company has built a machine learning-powered biomedicines platform with the potential to generate new drugs across a wide range of biologic modalities. This platform represents a potentially fundamental shift in what is possible in the field of biotherapeutic development. We pursue this audacious vision because we believe in the unique and revolutionary power of generative biology to radically transform the lives of billions, with an outsized opportunity for patients in need. We are seeking collaborative, relentless problem solvers that share our passion for impact to join us! Generate:Biomedicines was founded in 2018 by Flagship Pioneering and has received nearly $700 million in funding, providing the resources to rapidly scale the organization. The Company has offices in Somerville and Andover, Massachusetts with 300+ employees. The Role: Generate:Biomedicines is seeking an experienced and strategic cross-functional team leader accountable for designing and delivering our late-stage respiratory programs, including asthma and COPD. Reporting directly to the Chief Medical Officer, this is a senior level business leader who will recruit and develop a team of physicians and scientists with accountability for the global clinical trials, collaborating with PV to ensure rigorous safety oversight, data integrity, and strategic alignment. The ideal candidate is an MD with significant industry experience in respiratory medicine and a track record of driving executional excellence in pivotal trials. Here's how you will contribute: • Leads a high performing Respiratory Product Strategy Team (RPST) comprised of cross-functional leaders accountable for setting the strategy for the late stage respiratory programs • Direct management and development of medical monitors and clinical scientists • Develops high quality, ambitious development plans for asthma and COPD programs, aligned with late-stage and corporate objectives and compliant with all relevant regulations • Recruits, mentors and manages late-state clinicians and scientists • Collaborates with Head of Safety and PV to define risk-benefit profiles • Collaborates with Clinical operations and CRO to deliver study to timelines and budget • Oversees protocol development and clinical/scientific content for regulatory submissions and interactions • Provides medical leadership and awareness of evolving external landscape for late-stage clinical trials in respiratory diseases (asthma, COPD) • Drives development and refinement of Target Product Profiles (TPPs), Target Product Claims,and clinical development strategies • Oversee protocol development, study design, medical review of data, and safety monitoring • Serve as the primary medical contact for clinical sites, investigators, and regulatory bodies • Guide interactions with external stakeholders including KOLs, advisory boards, and CROs • Represent Generate externally at scientific, medical, and regulatory meetings Leadership Responsibilities • Hold teams to high standards for technical and collaborative performance • Build and develop a diverse, high-performing, and inclusive team culture • Promote enterprise thinking and cross-functional alignment with strategic goals • Communicate with clarity, courage, and empathy across all levels of the organization • Foster resilience, adaptability, and informed risk-taking in pursuit of innovation The Ideal Candidate will have: • MD (required), board certification in Pulmonology or Allergy and Immunology Medicine preferred • 10+ years of clinical development experience in the biopharma industry • Deep expertise in respiratory diseases (asthma, COPD) and late-stage clinical trials • Demonstrated success in leading pivotal global studies and regulatory interactions • Strong analytical, communication, and cross-functional leadership skills • Proven ability to influence internal and external stakeholders, including investigators and health authorities Education: • MD required; additional scientific training (e.g., fellowship, MPH) a plus Nice to Have (Optional): • Previous work in both large pharma and biotech settings • Knowledge of global regulatory requirements (e.g., FDA, EMA) • Recent successful BLA submission preferred Location: Somerville, MA / Andover, MA; remote (U.S.) optional with travel to HQ based on business needs. Why Join Us This is a unique opportunity to shape the future of respiratory medicine at a company pioneering Generative Biology™. You'll be empowered to lead transformative trials in a collaborative, mission-driven environment, surrounded by relentless problem solvers who are reimagining what's possible in drug discovery and development. #LI-KD1 #LI-RT1 Generate:Biomedicines is committed to equal employment opportunity regardless of race, color, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, disability, gender identity or Veteran status. Recruitment & Staffing Agencies: Generate:Biomedicines does not accept unsolicited resumes from any source other than candidates. The submission of unsolicited resumes by recruitment or staffing agencies to Generate:Biomedicines or its employees is strictly prohibited unless contacted directly by the Company's internal Talent Acquisition team. Any resume submitted by an agency in the absence of a signed agreement will automatically become the property of Generate:Biomedicines and the Company will not owe any referral or other fees with respect thereto. Apply tot his job