Jobs / United States / Sanofi US Services INC
Associate Medical Director
Sanofi US Services INC · 🇺🇸 2 Locations
Sponsorship verdict
Sponsorship possible
One solid signal, not two — worth applying, and worth asking about sponsorship early.
- Employer is on a government sponsor recordThe US Department of Labor certified 47 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 29 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
- The posting doesn’t mention sponsorshipSilence isn’t a refusal — ask the recruiter before investing much time.
- No salary bar for this routeH-1B has no fixed salary bar: the employer must pay at least the prevailing wage for the role and area. Cap-subject employers enter a lottery weighted by wage level. Source: https://www.federalregister.gov/documents/2025/12/29/2025-23853/weighted-selection-process-for-registrants-and-petitioners-seeking-to-file-cap-subject-h-1b, rules effective 2026-02-27.
- What Sanofi US Services INC paid sponsored hires in similar roles2 certified filings for “Associate Director” (Regulatory Affairs Managers) in MA: $147k–$147k, median $147k. Source: US Department of Labor LCA disclosure data (Oct 2025 – Jun 2026).
- Confirmed live todayWhen a source last listed this job as open.
US H-1B: cap-subject employers enter a lottery weighted by wage level — Level I gets 1 entry, Level IV gets 4 (DHS projected selection odds ≈15% at Level I to ≈61% at Level IV). Universities and non-profit research employers are cap-exempt. The $100,000 fee for new petitions from abroad is currently blocked by a court order (appeal pending).
A verdict summarises public evidence; it is not legal advice and never a guarantee — the employer and the immigration authority decide. Sign in to factor in where you can already work.
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Sponsor Radar — Sanofi US Services INC
The US Department of Labor certified 47 H-1B/E-3 labor condition applications for this employer between Oct 2025 and Jun 2026 (latest Jun 2026) — the step every H-1B hire needs first. USCIS also records 29 H-1B approvals in FY2023. Source: LCA disclosure data (US Department of Labor (OFLC)).
Past sponsorship or register membership never guarantees sponsorship for this vacancy or for you. Full Sponsor Radar for Sanofi US Services INC →
About the role
Job Title: Associate Medical Director • Location: Cambridge, MA About the job: As within our Global Respiratory Franchise, you’ll 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, you’ll help deliver breakthrough treatments that bring hope to patients with some of the highest unmet needs. About Sanofi: We’re an R&D-driven, AI-powered biopharma company committed to improving people’s 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 people’s 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 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 US Services and its U.S. affiliates are Equal Opportunity employers committed to a culturally inclusive workforce. All qualifie