Clinical Research Director

Sanofi; France; Híbrido; EUR 76.000 - 101.000; Jornada completa

Descripción de la vacante

Sanofi in Vitry-sur-Seine, France, is seeking a Clinical Research Director to lead clinical development strategy for assigned programs and drive execution across cross-functional teams. The role interfaces with Clinical Operations, Biostatistics, and Regulatory to shape development plans and ensure high-quality trial execution.

The ideal candidate will have oncology expertise, a track record in late-stage development, and strong collaboration skills to navigate regulatory and scientific

Formación

• MD with oncology training or fellowship, 4+ years of experience.
• Pharmaceutical industry experience preferred, with late-stage development.
• Experience designing and executing clinical trials with cross-functional teams.

Responsabilidades

• Lead clinical development strategy for programs and execute development plans.
• Oversee trial design, protocol reviews, and regulatory communications.
• Collaborate with Clinical Operations, Biostatistics, Translational Medicine and Regulatory.

Conocimientos

Oncology

Trial design

Cross-functional teamwork

Regulatory knowledge

Educación

MD with oncology experience

Descripción del empleo

## Clinical Research DirectorBewerben: Vitry-sur-Seine: Vollzeit: Heute ausgeschrieben: Enddatum: 31. Dezember 2026 (Noch 30+ Tage Zeit für Bewerbung): R2837532*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 MedicineParticipates 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 preparationScientific 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:**** *Oncology training (medical oncology or hematology/oncology fellowship) or MD with experience (4+ years) is required.****Languages:**** *Fluency in spoken and written English required (for global collaboration with US and European teams). French: Not required (nice to have for France-based positions). Spanish: Not required (nice to have for Spain-based positions).**What we offer**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.*Diversity und Inklusion sind in den Grundwerten von Sanofi verankert und spiegeln sich in unserer Arbeitsweise wider. Wir respektieren die Vielfalt unserer Belegschaft in Hinsicht auf ihre Herkunft, Erfahrungen und Lebensweisen. Wir erkennen die Bereicherung, die diese Vielfalt birgt, und fördern Inklusion sowie eine Arbeitsumgebung, in der diese Unterschiede sich weiter entwickeln können, zur Stärkung des Lebens unserer Mitarbeiter, Patienten und Kunden.The salary range for this position is :€76 000,00 - €101 333