Jobs / United States / Sanofi US Services INC
Clinical Research Director
Sanofi US Services INC · 🇺🇸 Vitry-sur-Seine
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).
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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
Clinical Research Director – Job description Job title: Clinical Research Director • Location : Vitry-sur-Seine, France • Hiring Manager : Ray Perez About the job Join the engine of Sanofi’s mission — where deep immunoscience meets bold, AI-powered research. In R&D, you’ll drive breakthroughs that could turn the impossible into possible for millions. Reporting to the Global Project Head, the CRD leads clinical trial strategy of assigned program(s) within the clinical development team, including interactions with Clinical Operations, Biostatistics, Regulatory, Translational Medicine, Project Management, New Product Planning and Pharmacovigilance to establish the development strategy and execute the development plan. The clinical development team further develops a compound through life cycle management. 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: Establishes or adapts clinical development plan for the program(s) including discussions with clinical investigators, advisors and regulatory authorities and plans contingencies. Leads, supports and oversees the execution of clinical development and studies activities, including but not limiting to: • Authors abbreviated protocol. • Reviews the final protocol and protocol amendments. • Reviews the Informed Consent Form, Written Subject Information and Trial Disclosure Form. • Reviews the study specific committee charters. Leads study specific committees with operational support. • Leads the clinical interpretation of study results, contributes to clinical study reports and clinical summaries. • Provides effective clinical guidance to other functions, including Clinical Operations, Biostatistics and Translational Medicine Participates and contributes to regulatory and safety documents and discussions • Reviews and/or contributes clinical sections of the Investigator Brochure, IND/IMPD filings, DSUR, development risk management plans • Contributes to the clinical sections of the NDA/CTD, Briefing packages for regulatory meetings, PSP/PIP • Participates in Advisory Committee preparation Scientific data evaluation and authorship • Authors clinical abstracts, presentations for conferences, and manuscripts, when appropriate • Supports the planning of advisory board meeting. Presents and discusses development strategy and clinical study result with external investigators and advisory boards, as appropriate About you Experience: • Oncology training (medical oncology or hematology/oncology fellowship) or MD with experience (4+ years) is required. • Pharmaceutical experience is required, 3+ years strongly preferred. • Experience in late-stage clinical development strongly preferred. • Demonstrated experience in clinical trial design and execution. • Proven track record of working effectively with multifunctional teams to achieve project milestones. • While industry experience is preferred, candidates with demonstrated excellence in academic clinical research and documented achievements may be considered with relatively less industry experience. Soft and Technical Skills: • Deep understanding of oncology, particularly solid tumor biology • Demonstrated ability to interact productively with external investigators • Demonstrated ability to work with a multifunctional team to achieve project milestones • Understanding of and willingness to meet applicable regulatory, quality and compliance standards Education: • Oncolog