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:
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.
Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people – people from different backgrounds, in different locations, doing different roles, all united by one thing: a desire to make miracles happen. So, let’s be those people.
At Sanofi, we provide equal opportunities to all regardless of race, colour, ancestry, religion, sex, national origin, sexual orientation, age, citizenship, marital status, ability or gender identity.
Watch our ALL IN video and check out our Diversity Equity and Inclusion actions at sanofi.com!