Senior Global Project Head, Neurology Development

Job Title: Senior Global Project Head, Neurology Development Location: Cambridge, MA Morristown, NJ 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 Senior Global Project Head (Sr GPH), Neurology Development role is a key position that leads early development activities in Neurology Development. The Sr GPH is responsible for shaping strategy as well as managing execution. This is a highly visible role that will work closely with the Research and Development Heads in the Therapeutic Area to build and renew the early portfolio in Neurology. Unlike other GPH roles, this role is focused on multiple projects from IND-enabling studies to first-in-human studies and successful proof-of-concept trials. New programs come from the internal research pipeline and from in-licensing. The Early Development GPH is a critical contributor for the selection of projects to move forward and will drive execution of projects until they have achieved proof of concept. In some cases, the GPH may transition to lead a later-stage development program. At Sanofi, we chase the miracles of science. Sanofi believes that the more we understand about disease pathogenesis in the human nervous system, the greater the chance we can produce life-changing therapies. Over the next five years, Sanofi plans to test in the clinic potentially disease-modifying treatments for diseases such as Multiple Sclerosis (MS), Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP), Alzheimer's Disease (ALZ), Parkinson's Disease (PD), Amyotrophic Lateral Sclerosis (ALS), as well as other CNS diseases. This Sr GPH role is focused on neurodegenerative diseases and particularly Alzheimer's Disease. Scientific excellence, integrative thinking, and strong interpersonal skills will be required to succeed. The Sr GPH reports to the TA Head, NOD. The impact on the organization is extensive due to the ability to influence disease area strategy and the network of collaborators from preclinical research to operational, regulatory, and commercial functions. Success in this role requires the ability to influence and lead at the highest possible level. The Sr GPH will be a critical member of the NOD leadership team and will be joining at a key point in time with the opportunity to build and influence the group. This role will require the ability to innovate and think creatively, engage multiple internal and external stakeholders, and make key decisions. The Sr GPH position requires achieving results through others and supporting the senior management team in achieving corporate goals. The Sr GPH establishes the goals for the global project team (GPT) and participates in strategic planning for, and oversight of, the clinical activities of his/her area of responsibility. The GPH will be responsible for interaction with regulatory authorities, approval of protocols, informed consent documents, clinical study reports, and product labels. In addition, the GPH will be responsible for the communication strategy and scientific disclosures, travel authorizations, and expense reports, and will interact with opinion leaders and consultants. Sanofi's Key Therapeutic Areas (TAs) include Immunology, Neurology & Ophthalmology Development (NOD), Rare and Rare Blood Diseases, and Vaccines. We help people with debilitating and complex conditions that are often difficult to diagnose and treat. We are dedicated to discovering and advancing new therapies, providing hope to patients and their families around the world. The NOD TA includes programs in Neuroimmunology, Neurodegeneration, and Ophthalmology, with therapeutic modalities encompassing Small Molecules, Biologics, and Gene Therapy. Sanofi has an internal research team, in addition to the Genomic Medicine Unit (GMU), which is committed to building the future pipeline. About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s 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 people’s lives.   Main Responsibilities: Scientific and Technical Expertise Has and maintains deep scientific, technical, and clinical expertise in Neurology Deep expertise in neurodegenerative diseases, especially Alzheimer's disease, is preferred Understands and keeps up to date with preclinical, clinical pharmacology, and other data relevant to the molecule of interest Critically reads and evaluates relevant medical literature with deep understanding of the data and status for competitive products Maintains visibility within the therapeutic area to maintain credibility with internal and external stakeholders Oversees development planning, execution, and budget Owns the overall program strategy and leads the international cross-functional team to meet program objectives Participates in life cycle management strategy planning in collaboration with marketing 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 Is responsible for annual budget deliverables Management and Career Development Ensures that team members are adequately qualified and trained in the tasks they are required to perform, including accountability and maintaining 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 Ensures timely submission and dissemination of clinical data Supports the planning of advisory board meetings Establishes and maintains appropriate collaborations with knowledge experts In addition to the above activities, the Sr GPH ensures that all activities of the GPT are conducted in compliance with current regulations, laws, and guidance from FDA, EMA, and CHMP, as well as with Sanofi's policies and procedures. About You Required Qualifications Bachelor's Degree required. Medical Doctor preferable, or PhD in relevant area 10 years of business-related experience is required 6+ years of experience in drug development within a therapeutic area is required Deep expertise in Early Development (Translational Medicine) is required Strong leadership skills to manage international, cross-functional teams of highly skilled individuals Experience in or demonstrated evidence for the capacity to lead and manage groups of professionals Excellent communication skills Fluent in English (verbal and written communication) Travel up to 25% is required Preferred Qualifications Strong scientific background with deep understanding of drug development; background in clinical development for Neurology is highly preferred Good 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 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 it’s 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. Sanofi Inc. 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. #GD-SA  #LI-SA     #LI-Hybrid #vhd  Pursue progress, discover extraordinary Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people. At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity. Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com! US and Puerto Rico Residents Only 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; natural or protective hairstyles; 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. North America Applicants Only The salary range for this position is: $266,250.00 - $443,750.00 All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the LINK.