Job Title: Global Medical Affairs Senior Director, Rhinology and Gastroenterology

Location: Cambridge, MA

About The Job

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.

Job Description

Sanofi is recruiting a new Global Leader in Medical Affairs to support product development through medical strategy and guidance for Dupilumab in the Global Immunology Franchise for Rhinology and Gastroenterology.

Dupilimab has the potential to change the landscape of EoE and CRSw/sNPs treatment and management and to be part of a paradigm shift.  

The new Leader will report directly into Head, Global Medical Affairs, Rhinology and Gastroenterology, and will be responsible for medical affairs activities for phase IV studies and Life Cycle management activities.   

With guidance from the Head, Global Medical Affairs Rhinology and Gastroenterology the new leader will be an integral part of building the global medical affairs strategy in line with the brand strategy supporting development and preparation for the launch of Dupilumab for Rhinology and Gastroenterology indications in partnership with Regeneron.  

The exceptional new hire will either have strong content area expertise in Rhinology and Gastroenterology or a desire to work in the immune-inflammation space with a solid working knowledge and background in Medical Affairs.    

Main Responsibilities:

• Support the Head of Global Medical Affairs Dupilumab Rhinology and Gastroenterology in the build and execution of Global Med Affairs strategy.

• Build and execute the Life Cycle management for Dupilumab Rhinology and Gastroenterology including pediatric indication; define and prioritize the future needs including new study ideas and tactics to prioritize the best areas for clinical trial investment.

• Collaborate with alliance partners at Regeneron: take a team-oriented approach to making sure strategy is clearly defined and consistent with relevant stakeholders in clinical development and commercial teams.

• Coordinate data gap analyses across the Regions and countries.

• Establish IEGP plans and supervise the implementation.

• Collaborate with the Alliance to execute the data generation activities in alignment with the Brand plan and Global Medical Affairs Plan.

• Lead and supervise analyses from the development program dupilumab for additional publications.

• Supervise physician/scientist in charge of the execution of the GMA LCM and data generation.

• Establish and maintain strong relationships with experts in the Rhinology and Gastroenterology field, academics and professionals and/or patient associations.  Prior knowledge of and established relationships with key opinion leaders in Rhinology and Gastroenterology considered an asset.

• Lead advisory boards or roundtables for anti-IL-4/IL-13 in Rhinology and Gastroenterology and gain strategic insights for medical, scientific, and development strategy.

• Give significant input to publications and co-author relevant abstracts.  Drive process of data dissemination and ensure that it is publicly presented in an appropriate and timely fashion and in a fair and balanced manner.

• Ensure the scientific integrity of sponsored and supported research, information, and relationships with healthcare providers and patient advocacy groups.

• Ensure a patient-centric approach to development of medical strategy both for product and device development as well as possible services which can enhance the value proposition of the product; Provide relevant feedback to market access teams to ensure optimal pricing and reimbursement strategy and inclusion of relevant endpoints in clinical trials.

• Travel required, comprising approximately 30%.

About You:

Basic Qualifications:

• MD required.

• Minimum 8 years’ experience in industry medical affairs.

• Prior experience in a Global or at least Regional medical affairs role.

• Prior experience in Immunology/Immune inflammation Medical affairs Life Cycle management.

• Experience working within an international company with a complex organizational environment; able to operate in a matrix team-oriented structure.

Preferred Qualifications:

• Global experience highly advantageous.

• Experience in Medical Affairs with Biologics (Dermatology, Rheumatology, Gastro others.) highly advantageous.

• Able to work on projects in coordination with the Alliance partner and establish excellent working relationships and credibility. 

• Excellent communication and presentation skills with the ability to present scientific data in a credible manner.  Able to interface professionally with a wide spectrum of internal and external academicians, agencies, and industry executives in the scientific/medical arena.

• Strong understanding of the pharmaceutical/biotech drug development and commercialization process.

• Leadership skills: personal style that includes a sense of urgency, as well as flexibility and ability to respond to rapidly changing environments and circumstances. 

• Collaborative and proactive, with a hands-on, roll-up-the sleeves style and attitude.

• Highest integrity; committed to ethics and scientific standards.

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.

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.

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Pursue progress, discover extraordinary

Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.

At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.

Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!

US and Puerto Rico Residents Only

Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; 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.