Respiratory Medical Director, Evidence & Strategy

Sanofi; Cambridge (MA); On-site; USD 149,000 - 215,000; Full time

Benefits offered by this job

Parental leave (gender-neutral)

Healthcare benefits

Wellbeing programs

Global collaboration opportunities

Job summary

Sanofi seeks an Associate Medical Director in Cambridge, MA to shape post‑marketing evidence for dupilumab across asthma and COPD. You will lead clinical and real‑world studies, coordinating with global experts to inform medical strategy and development priorities.

The role requires 5+ years in pharma/biotech R&D or Medical Affairs, plus a medical or scientific doctorate and proven ability to work in complex matrixed teams. Expect global collaboration and patient‑centered study design.

Qualifications

• 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 R&D, Medical Affairs, or related field.
• Experience in complex matrixed organizational environments.
• Strong scientific communication and presentation skills.

Responsibilities

• Support the development and execution of 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.
• Collaborate with regional affiliates to align evidence generation with the Global Medical Plan.
• Evaluate external sponsored research initiatives ensuring scientific rigor and relevance.
• Build relationships with respiratory experts, academics, patient groups, and key opinion leaders.

Skills

Scientific communication

Cross-functional leadership

Clinical study design

Education

MD/PhD/PharmD or Master's in a relevant scientific field

Job description

Sanofi seeks an Associate Medical Director in Cambridge, MA to shape post‑marketing evidence for dupilumab across asthma and COPD. You will lead clinical and real‑world studies, coordinating with global experts to inform medical strategy and development priorities.

The role requires 5+ years in pharma/biotech R&D or Medical Affairs, plus a medical or scientific doctorate and proven ability to work in complex matrixed teams. Expect global collaboration and patient‑centered study design.