Global Project Head, Solid Tumor Antibody Drug Conjugates (ADCs)

Job Title Global Project Head, Solid Tumor Antibody Drug Conjugates (ADCs) Location Cambridge, MA / Morristown, NJ About The Job Join the engine of Sanofis mission where deep immunoscience meets bold, AI-powered research. In R&D, youll drive breakthroughs that could turn the impossible into possible for millions. About Sanofi We’re an R&D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve peoples lives. Key Responsibilities The Global Project Head (GPH) drives worldwide clinical development and life cycle management for a late-stage Sanofi Antibody Drug Conjugate (ADC) compound within Solid Tumor Oncology. The GPH leads the GPT (global product team) to ensure optimal development of the global compound development strategy in collaboration with the GBT (global brand team). In this assignment the GPH will be accountable for the compound clinical development strategy and execution, with a focus on studies for regulatory purposes and including budget planning. The GPH will collaborate with the Principal Clinical Lead (PCL) and Global Project Manager (GPM) to lead the cross-functional GPT (which includes translational, regulatory, drug manufacturing, safety, medical and commercial compound leads), to ensure correct planning and implementation of end‑to‑end compound strategy. The GPH will represent the Clinical Development function at the cross‑functional GBT responsible for commercial brand strategy. The GPH will partner with the PCL to present and discuss development strategy with key internal stakeholders, external investigators and advisory boards, and worldwide regulatory authorities. The Global Project Head is also an essential contributor to Sanofi Solid Tumor Oncology and cross‑asset Disease Area strategies. The GPH will be responsible for the Clinical Development assessment of external business development opportunities in Hematopoietic Stem Cell Transplantation, and, if applicable, become responsible for the implementation of this Development strategy. Requirements About You MD or PhD 7 or more years of experience in clinical development in Solid Tumor Oncology, in the biotech or pharmaceutical industry Thorough understanding of global drug development and functional roles and responsibilities Proven effective leadership of high‑performing cross‑functional clinical development teams Experience in successful submissions for marketing authorization Excellent written and verbal communication skills 20% travel domestic and international Preferred Qualifications Experience leading pivotal trials to support submission for regulatory approval in solid tumor oncology. Strong leadership and clinical expertise in the field, to enable effective international collaboration with external and internal stakeholders. Experience preparing regulatory submissions, and discussion / negotiation with health authorities. Experience collaborating with commercial and medical functions in launch and/or post‑launch settings Experience working in a matrix environment Ability to integrate new information, adapt, and change direction in response evolving data and/or external landscape (CI, regulatory, etc) Ability to develop strong networks internally and externally. Experience in regional alliance partnerships or co‑development Strong interpersonal, cross‑functional, and cross‑cultural communication skills Ability to define clear and challenging, but realistic, goals. Ability to assess the balance of investment and deliverables. Results and customer focused. Organizational awareness. Why Choose Us? Bring the miracles of science to life alongside a supportive, future‑focused team. Discover endless opportunities to grow your talent and drive your career, whether its through a promotion or lateral move, at home or internationally. Enjoy a thoughtful, well‑crafted rewards package that recognizes your contribution and amplifies your impact. Take good care of yourself and your family, with a wide range of health and wellbeing benefits including high‑quality healthcare, prevention and wellness programs and at least 14 weeks gender‑neutral parental leave. Equal Opportunity Statement Sanofi US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law. All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here. #J-18808-Ljbffr BioSpace