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Sanofi Group Rare Hematology Life-cycle management Global Medical Lead in Cambridge, Massachusetts

Position Overview:

The Rare Hematology LCM Global Medical Director will report to the Head of Medical Rare Hematology and will be part of the Global Medical Affairs Rare Disease Team.

This person will be responsible for setting a LCM strategy and lead medical affairs data generation activities for Gaucher & ASMD diseases. The LCM Global Medical Director will provide oversight to the Gaucher registry, develop protocols and manage company sponsored studies, and provide medical expertise for real-world evidence studies in coordination with other members of the medical team.

The position requires the ability to work effectively in a highly matrixed environment; highly team oriented with outstanding interpersonal skills and ability to collaborate effectively with other groups will be needed, as will a demonstrated ability to see the big picture while not losing focus on project specifics; the ability to both develop project strategies and execute project details.

A strong commitment to achieving corporate objectives while maintaining the highest ethical, regulatory and scientific standards is required.

In the day to day business, the person will build strategic plans, supervise the implementation and execution of the medical affairs activities across broad range of countries in US, Europe, and JPAC and Emerging Markets.

In addition, He/She will work closely with the leadership of Sanofi Genzyme’s Research, Clinical Development, Commercial, Health Economics and Value and Access and Product Management functions to support optimal life cycle management in Rare Hematology (Gaucher/ASMD).

Key Responsibilities:

  • Oversee management of strategy around Investigator Sponsored Studies and Phase IV Medical Affairs Studies, including membership in the Scientific Review Committee to ensure that the LCM strategy is clearly defined and consistent with the clinical development and strategic objectives for each product, and that appropriate processes are in place for review, approval, management and support of studies that are scientifically sound.

  • Lead, along with colleagues in Global Scientific Communication, management of publication planning and execution to ensure that all data on Sanofi Genzyme products generated by company or investigator sponsored trials is publicly presented in an appropriate and timely fashion and in a fair and balanced manner.

  • Oversee management of funding for CME, grants, and sponsorships to ensure that funds are allocated appropriately to activities consistent with the clinical development and commercial objectives of the business, and that review and approval processes are in place to maintain strict compliance with all federal regulations.

  • Responsibility and accountability for the financial management and reporting requirements for medical affairs, including supporting the Finance reporting process with accurate and timely data and assumptions as needed to support budgeting, forecasting and long-range planning for the business units. Manage the budget.

  • Ensure that medical guidance is provided to marketing teams.

  • Participate in relevant Sanofi Genzyme Product Teams to provide expertise and ensure alignment of medical affairs with clinical development and commercial activities.

  • Provide leadership in identifying needs for post-marketing clinical trials and registries and oversee their management and execution.

  • Represent the function at medical meetings, advisory boards, outreach meetings at key institutions, and in interactions with KOLs.

  • Travels regularly (both internationally and within the US) as necessary.

Basic Qualifications:

  • M.D. with significant pharma medical affairs experience preferred or equivalent industry experience.

  • Significant leadership and management experience in Medical Affairs or other aspects of the life sciences sector.

  • Experience in clinical development studies and post-marketing Medical Affairs.

  • Experience in both clinical research and patient care.

  • Demonstrated ability to work effectively in a matrixed environment.

  • Proficient in public speaking.

  • Five years of experience in the biotech or pharmaceutical industry.

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse 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.



At Sanofi diversity and inclusion is foundational to how we operate and embedded in our Core Values. We recognize to truly tap into the richness diversity brings we must lead with inclusion and have a workplace where those differences can thrive and be leveraged to empower the lives of our colleagues, patients and customers. We respect and celebrate the diversity of our people, their backgrounds and experiences and provide equal opportunity for all.