Global Project Head (GPH), Ophthalmology

Job Title Global Project Head (GPH), Ophthalmology Location Morristown, NJ / Cambridge, MA About the Job Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. The Ophthalmology Development Global Program Head (GPH) is a key position that oversees early and late development activities and is responsible for shaping asset strategy as well as managing execution. This role is focused on multiple projects from IND-enabling studies, first in human studies to proof of concept and registrational trials. It is a highly visible role that will work closely with the Research and Development teams and leaders in the therapeutic area to build and expand the portfolio in Ophthalmology. Main Responsibilities Owns the overall program strategy and leads the international cross‑functional team to meet program objectives. Demonstrates deep scientific, technical and clinical expertise in Ophthalmology and/or gene therapy. Oversees development planning, execution and budget; participates in life cycle management strategy planning in collaboration with commercial teams. Proposes strategies for interactions with health authorities; establishes project goals in alignment with functional resource allocation, goals and objectives. Responsible for generating support and implementation of clinical studies; ensures operational plans are integrated across all functions. Responsible for annual budget deliverables; understands and keeps updated with the pre‑clinical, clinical pharmacology and data relevant to the molecule of interest. Critically reads and evaluates relevant medical literature with deep understanding of the data and status from competitive products; maintains visibility within the therapeutic area to maintain credibility with internal and external stakeholders. Demonstrates excellent analytical and judgement skills. Manages and leads the team; ensures team members are adequately qualified and trained; leads cross‑functional team with appropriate responsibility and accountability across team members; ensures compliance training for direct reports. Works cross‑functionally to select appropriate team members; sets team’s objectives, and works closely with direct reports to create individual performance and development goals. Regulatory responsibilities: ensures clinical data meets all necessary regulatory standards; supports registrations, label submissions and modifications; manages Advisory Committee preparation and participation. Scientific data dissemination: ensures timely submission and dissemination of clinical data; supports the planning of advisory board meetings; establishes and maintains collaborations with knowledge experts. Ensures all activities of the GPT are conducted in compliance with current regulations, laws, and guidance from FDA, EMeA, CHMP, as well as with Sanofi’s policies and procedures. Required Qualifications Medical Doctor, PharmD or PhD in a relevant area. Deep expertise in Ophthalmology or Retina/Gene Therapy Clinical development. 6 years of experience in drug development or 10 years in the industry, within therapeutic area. Excellent communication skills; fluent in English (verbal and written). Experience in or demonstrated evidence for the capacity to lead and manage groups of professionals. Strong leadership skills to manage international, cross‑functional teams of highly skilled individuals. Travel up to 20%, domestic and international. Preferred Qualifications Strong scientific background with deep understanding of drug development; background in ocular gene therapy clinical development is highly preferred. Strong networking ability in cross‑cultural environment. Strong interpersonal, communication, presentation, and negotiation skills across all levels of the organization. In depth knowledge of global drug development activities including the development of other healthcare solutions along the whole value chain from research up to market access. Skilled in project and/or budget/resource management. Strategic thinking in combination with understanding science and technologies. Performance oriented with ability to work along agreed timelines and a focus on strategy and execution. Outstanding communicator. Excellent problem‑solving, conflict‑resolution and decision‑making skills. Benefits Competitive salary ranging from $232,500.00 to $335,833.33, commensurate with experience. Eligible for Company employee benefit programs. Benefits include high‑quality healthcare, prevention and wellness programs, and at least 14 weeks’ gender‑neutral parental leave. Equal Opportunity Sanofi Inc. and its U.S. affiliates are Equal Opportunity and affirmative action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race, color, creed, religion, national origin, age, ancestry, nationality, marital status, sex, gender, gender identity, sexual orientation, disability, veteran status, or any other characteristic protected by law. #J-18808-Ljbffr