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Sanofi

Global Program Head, Neurology (Hiring Immediately)

Sanofi, Cambridge, Massachusetts, us, 02238

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Job title:

Global Program Head, Neurology

Please make an application promptly if you are a good match for this role due to high levels of interest. Location:

Cambridge, MA About the job Are you ready to shape the future of medicine? The race is on to speed up drug discovery and development to find answers for patients and their families. Your skills could be critical in helping our teams accelerate progress. The Global Program Head (GPH) is a key position that oversees key development activities in the Neurology & Ophthalmology Development (NOD) and is responsible for shaping strategy as well as managing execution. This is a highly visible role will work closely with the Development Heads in the Therapeutic Area to build and expand the portfolio in Neurology. This role is focused on leading global program teams (GPTs) and is responsible for the strategy and development activities of neurology clinical stage assets. 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. Sanofi plans to regularly test in the clinic potentially disease-modifying treatments for Multiple Sclerosis, Chronic Inflammatory Demyelinating Polyradiculopathy (CIDP), Parkinsons Disease, and Alzheimers 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 several direct reports of medical directors and clinical scientists based on program needs. The impact on the organization is extensive due to the ability to influence 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 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 GPH position requires achieving results through others and supporting the senior management team in achieving corporate goals. The GPH establishes the goals for the global project team (GPT) and participates in strategic planning for, and oversight of, the clinical and research activities of his/her area of responsibility. The GPH will be delegated such responsibilities as interaction with regulatory/health 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 and travel authorizations, expense reports, and will interact with opinion leaders and consultants. Sanofis Research and Development: Sanofis specialty care is focused on four Therapeutic Areas: Rare and Rare Blood Diseases, Neurology & Ophthalmology Development (NOD), Immunology, and Oncology. 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 includes programs in Multiple Sclerosis, Neuroimmunology, Neurodegeneration, and Ophthalmology, with therapeutic modalities encompassing Small Molecules, Biologics, and Gene Therapy. Sanofi has a large internal research team in addition to the Genomic Medicine Unit (GMU), which are committed to building the future pipeline in various neurological and ophthalmological diseases. We are an innovative global healthcare company with one purpose: to chase the miracles of science to improve peoples lives. Were also a company where you can flourish and grow your career, with countless opportunities to explore, make connections with people, and stretch the limits of what you thought was possible. Ready to get started? Main Responsibilities: Scientific and technical Expertise Has and maintains deep scientific, technical and clinical expertise in Neurology

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

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 task they are required to perform. Including accountability and maintaining compliance training for direct reports

Works cross functionally to select appropriate team members

Sets teams 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 appropriate collaborations with knowledge experts

In addition to the above activities the GPH ensures that all activities of the GPT are conducted in compliance with current regulations, laws, and guidance from FDA, EMeA, and CHMP, as well as with Sanofis 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

6+ yrs of experience in drug development within a therapeutic area

Strong leadership skills to manage international, cross-functional teams of highly skilled individuals

Strong prior regulatory interaction experience

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%

Preferred Qualifications Strong scientific background with deep expertise in Late Development and Medical Sciences; clinical development experience in Neurology is highly preferred.

Prior development experience in multiple sclerosis is 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 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