Sanofi Group
Job Title:
Global LCM Senior Medical Director
Location:
Morristown, NJ Cambridge, MA
About the Job This role is part of the Global Medical Affairs team for Neurology within Specialty Care Medical Affairs. Our Medical Affairs function serves as key strategic partners for commercial, regulatory, R&D, market access and external affairs to develop and launch first‑in‑class and best‑in‑class therapeutic solutions that address highest unmet needs.
Within Global Medical Affairs Neurology, we are proud to support Sanofi’s purpose of "Chasing the miracles of science to improve people’s lives" and to improve the health and lives of people with neurological disorders around the world.
Reporting to the Global Medical Lead for Tolebrutinib, the Global Senior Medical Director for Life Cycle Management (LCM) will oversee all data generation activities (phase IV interventional studies, RWE studies, ESR) for Tolebrutinib, from the strategy (data gap analysis, IEGP, study design) to the execution (contracting, study enrollment and follow‑up, budget tracking). In addition, the LCM senior director will be the global medical point of contact for the GPT for LCM activities and will oversee, in close collaboration with the scientific communication head and directors, the scientific publication and communication strategy.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main Responsibilities
Lead the strategy of global medical‑lead studies for Tolebrutinib, including the management of the study Steering Committee, development of the study results analysis and dissemination plan (primary and secondary results), interaction with global regulatory agencies and collaboration with the global operational and local medical teams to support study enrollment.
Provide leadership to the Tolebrutinib life‑cycle management strategy, perform yearly global data gap analysis and identify needs for high‑value medical‑affairs–driven studies and registries, and oversee their management and execution in accordance with established budgets and timelines.
Develop medical strategies to obtain relevant evidence from investigator‑sponsored studies, including Real World Evidence (in collaboration with HEVA), consistent with data generation objectives for Tolebrutinib.
Support the Global Project and Regulatory teams to interact and respond to requests from global regulatory agencies (FDA, EMA and other agencies).
Co‑lead with the scientific communication head and lead the global data dissemination plan for Tolebrutinib, including publications and global congress abstracts for the evidence generation pipeline.
Collaborate with the Tolebrutinib Global Medical Directors for the definition of the Tolebrutinib global medical strategy and the execution of key global medical tactics (such as symposiums, advisory boards, and field medical insights).
Support sharing of best practices between priority countries and others.
Ensure a patient‑centric approach to the development and execution of projects under your accountability.
Adhere strictly to compliance rules, regulatory, access and ethical requirements.
About You Experience
Minimum 10 years’ local/global experience in industry medical or R&D, with a solid track record of achievement in Medical Affairs in the biotech/pharma industry. Launch experience is preferred.
Suitable prior experience with global medical or clinical evidence generation activities, publications, scientific communications and experience within Neurology would be advantageous.
Experience working in an international multi‑country setting is preferred.
Significant line and matrix management experience, including strong transversal collaboration with key functions such as Research, Clinical Development, Scientific Communications, Commercial, Health Economics, Value and Access and Product Management functions.
Leadership Skills
Strategic thinking: ability to disrupt the status quo with innovation while remaining pragmatic and focused on priorities. When under pressure, ability to bring others along to explain how strategic ideas fit into the larger context, and approach challenges thoroughly with a broad view, considering different potential outcomes.
Result orientation: driven to develop and execute optimal strategy meeting corporate objectives, while creating pragmatic solutions. Comfortable with ambiguity and able to adapt with agility, take calculated risks and anticipate potential issues.
People leadership: ability to lead through influence, inspire teams, engage and leverage everyone’s strengths while being highly self‑aware. Set high standards and expectations, communicate proactively, collaborate and remain approachable, and provide meaningful feedback, coaching and support.
Relationships and influence: ability to empower and recognize others to create powerful relationships and networks. Effective stakeholder management, politically astute and role‑model teamwork and collaboration.
Highest ethical, regulatory and scientific standards.
Technical Skills
Education: MD, PhD, PharmD, or equivalent scientific degree.
Languages: Fluent in English.
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.
US and Puerto Rico Residents Only
North America Applicants Only
The salary range for this position is:
$202,500.00 – $292,500.00
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 Inc. and its U.S. affiliates are Equal Opportunity and Affi… (include full EEO statement here). All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; ... (full statement continues).
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering, and stand by the few who suffer from rare diseases and the millions with long‑term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting www.sanofi.com.
#J-18808-Ljbffr
Global LCM Senior Medical Director
Location:
Morristown, NJ Cambridge, MA
About the Job This role is part of the Global Medical Affairs team for Neurology within Specialty Care Medical Affairs. Our Medical Affairs function serves as key strategic partners for commercial, regulatory, R&D, market access and external affairs to develop and launch first‑in‑class and best‑in‑class therapeutic solutions that address highest unmet needs.
Within Global Medical Affairs Neurology, we are proud to support Sanofi’s purpose of "Chasing the miracles of science to improve people’s lives" and to improve the health and lives of people with neurological disorders around the world.
Reporting to the Global Medical Lead for Tolebrutinib, the Global Senior Medical Director for Life Cycle Management (LCM) will oversee all data generation activities (phase IV interventional studies, RWE studies, ESR) for Tolebrutinib, from the strategy (data gap analysis, IEGP, study design) to the execution (contracting, study enrollment and follow‑up, budget tracking). In addition, the LCM senior director will be the global medical point of contact for the GPT for LCM activities and will oversee, in close collaboration with the scientific communication head and directors, the scientific publication and communication strategy.
We are an innovative global healthcare company, committed to transforming the lives of people with immune challenges, rare diseases and blood disorders, cancers, and neurological disorders. From R&D to sales, our talented teams work together, revolutionizing treatment, continually improving products, understanding unmet needs, and connecting communities. We chase the miracles of science every single day, pursuing progress to make a real impact on millions of patients around the world.
Main Responsibilities
Lead the strategy of global medical‑lead studies for Tolebrutinib, including the management of the study Steering Committee, development of the study results analysis and dissemination plan (primary and secondary results), interaction with global regulatory agencies and collaboration with the global operational and local medical teams to support study enrollment.
Provide leadership to the Tolebrutinib life‑cycle management strategy, perform yearly global data gap analysis and identify needs for high‑value medical‑affairs–driven studies and registries, and oversee their management and execution in accordance with established budgets and timelines.
Develop medical strategies to obtain relevant evidence from investigator‑sponsored studies, including Real World Evidence (in collaboration with HEVA), consistent with data generation objectives for Tolebrutinib.
Support the Global Project and Regulatory teams to interact and respond to requests from global regulatory agencies (FDA, EMA and other agencies).
Co‑lead with the scientific communication head and lead the global data dissemination plan for Tolebrutinib, including publications and global congress abstracts for the evidence generation pipeline.
Collaborate with the Tolebrutinib Global Medical Directors for the definition of the Tolebrutinib global medical strategy and the execution of key global medical tactics (such as symposiums, advisory boards, and field medical insights).
Support sharing of best practices between priority countries and others.
Ensure a patient‑centric approach to the development and execution of projects under your accountability.
Adhere strictly to compliance rules, regulatory, access and ethical requirements.
About You Experience
Minimum 10 years’ local/global experience in industry medical or R&D, with a solid track record of achievement in Medical Affairs in the biotech/pharma industry. Launch experience is preferred.
Suitable prior experience with global medical or clinical evidence generation activities, publications, scientific communications and experience within Neurology would be advantageous.
Experience working in an international multi‑country setting is preferred.
Significant line and matrix management experience, including strong transversal collaboration with key functions such as Research, Clinical Development, Scientific Communications, Commercial, Health Economics, Value and Access and Product Management functions.
Leadership Skills
Strategic thinking: ability to disrupt the status quo with innovation while remaining pragmatic and focused on priorities. When under pressure, ability to bring others along to explain how strategic ideas fit into the larger context, and approach challenges thoroughly with a broad view, considering different potential outcomes.
Result orientation: driven to develop and execute optimal strategy meeting corporate objectives, while creating pragmatic solutions. Comfortable with ambiguity and able to adapt with agility, take calculated risks and anticipate potential issues.
People leadership: ability to lead through influence, inspire teams, engage and leverage everyone’s strengths while being highly self‑aware. Set high standards and expectations, communicate proactively, collaborate and remain approachable, and provide meaningful feedback, coaching and support.
Relationships and influence: ability to empower and recognize others to create powerful relationships and networks. Effective stakeholder management, politically astute and role‑model teamwork and collaboration.
Highest ethical, regulatory and scientific standards.
Technical Skills
Education: MD, PhD, PharmD, or equivalent scientific degree.
Languages: Fluent in English.
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.
US and Puerto Rico Residents Only
North America Applicants Only
The salary range for this position is:
$202,500.00 – $292,500.00
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 Inc. and its U.S. affiliates are Equal Opportunity and Affi… (include full EEO statement here). All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; ... (full statement continues).
Sanofi is dedicated to supporting people through their health challenges. We are a global biopharmaceutical company focused on human health. We prevent illness with vaccines, provide innovative treatments to fight pain and ease suffering, and stand by the few who suffer from rare diseases and the millions with long‑term chronic conditions.
With more than 100,000 people in 100 countries, Sanofi is transforming scientific innovation into healthcare solutions around the globe. Discover more about us visiting www.sanofi.com.
#J-18808-Ljbffr