Senior Global Project Head, Neurology Development

Sanofi•Morristown, MA

14d

About The Position

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) in Neurology, with a focus on multiple sclerosis, is a key position that oversees critical development activities in the Neurology & Ophthalmology Development (NOD) Therapeutic Area (TA). The Sr GPH is responsible for shaping strategy as well as managing execution. This highly visible role will work closely with the TA Head to build and expand the portfolio in Neurology. This role is focused on leading a global program team (GPT) responsible for a Phase 3 stage multiple sclerosis program. The Sr GPH should also contribute to the strategy and development activities end-to-end from research to clinical stage assets for neuroimmunology and multiple sclerosis. At Sanofi, we chase the miracles of science. Sanofi believes that the more we understand disease pathogenesis in the human nervous system, the greater the chance we can produce life-changing therapies. Sanofi plans to regularly test in the clinic potentially disease-modifying treatments for diseases such as Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculopathy (CIDP), Parkinson's Disease, and Alzheimer's disease. Scientific excellence, integrative thinking, and strong interpersonal skills will be required to succeed in this role. The plan is for the incumbent to have a senior role and manage several direct reports of medical directors and clinical scientists. The impact on the organization is extensive due to the ability to lead program strategy and the network of collaborators from 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 a 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 GPT and leads the strategic planning for, and oversight of, the clinical and other activities of his/her area of responsibility. The Sr GPH responsibilities will include interactions with regulatory authorities, approval of protocols, informed consent documents, clinical study reports, and product labels. In addition, the Sr GPH will be responsible for the communication strategy and scientific disclosures and travel authorizations, expense reports, and will interact with opinion leaders and consultants.

Requirements

Medical Doctor (MD) required.
Minimum of 10 years of clinical, scientific, or industry experience required, preferably within the field of neurology
Fluent in English (verbal and written communication)
Ability to travel up to 25% domestic and international required, including for scientific congresses, health authority meetings, advisory boards, investigator/site meetings and internal meetings. Approximately 50% domestic, 50% international.

Nice To Haves

Strong scientific and academic background with deep understanding of disease mechanisms, including in-depth understanding of neuroimmunology diseases
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
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 health care 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

Responsibilities

(60%) Scientific and Technical Leadership Maintains advanced scientific, technical, and clinical expertise in Neurology. Reviews and analyzes pre-clinical, clinical pharmacology, and molecular data on a weekly basis to inform program strategy Conducts critical evaluation of medical literature monthly, providing comprehensive competitive intelligence reports to leadership team Maintains visibility within the therapeutic area through quarterly participation in scientific conferences and monthly engagement with key opinion leaders Directs development planning, execution, and manages program with annual budgets ranging from $50-100 million Develops and implements overall program strategy while leading international cross-functional teams of currently 8 direct reports, and 10-15 other key teams members from other functions, to achieve program milestones Coordinates life cycle management strategy planning quarterly in collaboration with marketing teams Formulates and presents strategies for health authority interactions, including FDA and EMA meetings Establishes specific project goals monthly in alignment with functional resource allocation and corporate objectives Oversees generation and implementation of clinical studies, managing 3-5 concurrent Phase II/III trials Coordinates operational plans across all functions on a bi-weekly basis through cross-functional team meetings Manages and delivers annual budget targets with accountability for cost control and resource optimization
(20 %) Management and Career Development Validates that team members possess required qualifications and training through quarterly competency assessments, maintaining 100% compliance training completion for 5-8 direct reports Collaborates cross-functionally to recruit and select appropriate team members for specialized roles Establishes team objectives quarterly and conducts monthly one-on-one meetings with direct reports to develop individual performance and career development goals
(10%) Regulatory Responsibilities Reviews and validates clinical data compliance with FDA, EMA, and ICH regulatory standards through weekly data review meetings Coordinates registrations, label submissions, and modifications with regulatory teams on established timelines Directs Advisory Committee preparation activities and participates in regulatory meetings as company representative Monitors timely submission and dissemination of clinical data according to regulatory timelines Coordinates planning of advisory board meetings quarterly with key opinion leaders Develops and maintains strategic collaborations with external knowledge experts and academic institutions
(10%) Compliance Verifies 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 through monthly compliance audits and quarterly regulatory assessments.

Benefits

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.

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