Associate Medical Director

BioSpace; Cambridge (MA); On-site; USD 180,000 - 240,000; Full time

Job summary

BioSpace in Cambridge, MA is seeking an Associate Medical Director to lead post-marketing medical evidence generation for dupilumab in asthma and COPD. You will design and execute clinical and real-world studies, partnering with global experts in a dynamic, matrixed organization to advance patient outcomes.

The role emphasizes scientific communication, collaboration with regional affiliates, and advisory board support to shape medical and development priorities, with a patient-centered approach

Qualifications

• Graduate degree in a relevant scientific or medical discipline.
• Minimum of 5 years of industry experience in the pharmaceutical, biopharmaceutical, or biotechnology industry in R&D, Medical Affairs, or a related field.
• Experience operating within complex matrixed organizational environments.
• Strong scientific communication and presentation skills.

Responsibilities

• Support the Integrated Evidence Generation Plan and Global Medical Strategy for dupilumab in asthma and COPD.
• Design Phase IV study synopses, including interventional, observational, and real-world evidence studies.
• Partner with regional and local affiliates to support their evidence generation plans and studies, ensuring alignment with the Global Medical Plan.
• Evaluate and support external sponsored research initiatives, maintaining scientific rigor and strategic relevance.
• Build and maintain strong relationships with respiratory experts, academics, patient associations, and key opinion leaders to inform clinical development strategy.
• Support advisory boards and roundtables to gather strategic insights that shape medical, scientific, and development priorities.
• Ensure a patient-centric approach in the design and execution of all clinical studies, collaborating closely with the alliance to deliver on shared objectives.

Skills

Scientific communication

Presentation skills

Matrixed environment experience

Education

MD/PhD/PharmD/Master in a scientific field

Job description

About The Job

As within our Global Respiratory Franchise, youll play a pivotal role in shaping post-marketing medical evidence generation for dupilumab across asthma and COPD indications. This is a unique opportunity to drive meaningful patient impact through rigorous clinical and real-world evidence, while collaborating with world-class experts across a dynamic, matrixed global organization. Ready to get started?

Job Title: Associate Medical Director

Location: Cambridge, MA

About The Job

As within our Global Respiratory Franchise, youll play a pivotal role in shaping post-marketing medical evidence generation for dupilumab across asthma and COPD indications. This is a unique opportunity to drive meaningful patient impact through rigorous clinical and real-world evidence, while collaborating with world-class experts across a dynamic, matrixed global organization. Ready to get started?

Join the team transforming care for people with immune challenges, rare diseases, cancers, and neurological conditions. In Specialty Care, youll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs.

About Sanofi

Were an R&D-driven, AI-powered biopharma company committed to improving peoples lives and delivering compelling growth. Our deep understanding of the immune system and innovative pipeline enables us to invent medicines and vaccines that treat and protect millions of people around the world. Together, we chase the miracles of science to improve peoples lives.

Main Responsibilities

• Support the development and execution of the Integrated Evidence Generation Plan and Global Medical Strategy for dupilumab in asthma and COPD.
• Design clinical study synopses for Phase IV studies, including both interventional, observational, and real-world evidence (RWE) studies.
• Partner with regional and local affiliates to support their evidence generation plans and studies, ensuring alignment with the Global Medical Plan.
• Evaluate and support external sponsored research initiatives, maintaining scientific rigor and strategic relevance.
• Build and maintain strong relationships with respiratory experts, academics, patient associations, and key opinion leaders to inform clinical development strategy.
• Support advisory boards and roundtables to gather strategic insights that shape medical, scientific, and development priorities.
• Ensure a patient-centric approach in the design and execution of all clinical studies, collaborating closely with the alliance to deliver on shared objectives.

About You

Basic Requirements

• Graduate degree in a relevant scientific or medical discipline (MD, PhD, PharmD, or Master's in a relevant scientific field)
• Minimum of 5 years of industry experience in the pharmaceutical, biopharmaceutical, or biotechnology industry in R&D, Medical Affairs, or a related field
• Experience operating within complex matrixed organizational environments
• Strong scientific communication and presentation skills

Preferred Qualifications

• Demonstrated experience in clinical trial methodology, design, and execution including Phase IV, observational, or real-world evidence studies
• Experience in a global or regional medical or clinical development role
• Experience in biologics within respiratory, immunology, or immune inflammation therapeutic areas
• Experience with dupilumab, asthma, or COPD
• Experience in alliance or partnership settings

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 its through a promotion or lateral move, at home or internationally.
• Enjoy a thoughtful, well-crafted rewards package that recognises 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 US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive 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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All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs, and additional benefits information can be found here.