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. 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. Responsibilities 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 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 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 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 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 Salary range: $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. 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. #J-18808-Ljbffr