Job Title: Senior Clinical Research Director
Location: Cambridge, MA, Morristown, NJ
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.
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:
The role of the Senior CRD is to:
1. Act as a mentor for other CRDs and Clinical Scientists on a same project/TA
2. Collaborate with functions to ensure uniform, aligned operational approach (e.g harmonizing study documents, ES, protocols, etc). As relevant, within a project, ensure leadership, build consensus, coordinate action plans with other CRDs and stakeholders to resolve project-related study issues, anticipates potential issues (sharing lessons learned) across the project or study teams. He/she raises study or project-level issues to TA Heads, as relevant and shares relevant information within and beyond Project teams.
3. Take on as necessary the CRD role:
Provide medical expertise to the clinical studies (except select Exploratory Pharmacology studies) and/or registries (eg: protocol, Key Results, Clinical Study Report)
Support other clinical development activities (e.g. pressure test and cluster feasibility, medical review and validation of clinical data, study risk assessment)
Contribute to the clinical part of submission dossier for their projects: Common Technical Document for FDA & EMA submission, filing in Japan and China andanswers to questions from health authorities
Provide appropriate medical input & support for all activities related to clinical studies such as medical training, feasibility, medical review of data, medical information for the study team, medical advisors/Clinical Project Leaders from Clinical Study Units, and investigators
Be the medical reference in the Clinical Study team, ensuring the medical relevance of the clinical data
Interact with other CRDs in the project, Global Project Head, The PV Rep, Regulatory and other key functional reps
About You
Experience
4. Understanding of pharmaceutical product development and life cycle management gained through ~4 years of clinical development and medical experience
5. Excellent Scientific and medical / clinical expertise
6. Excellent expertise in clinical development and methodology of clinical studies
7. Excellent communication skills (verbal and written) for interactions across functional areas and for interactions with key regulatory agencies
8. Demonstrated capability to challenge decision and status quo with a risk-management approach
9. Ability to negotiate to ensure operational resources are available for continued clinical conduct
10. Fluency in written and spoken English
11. Excellent Teaching skills, demonstrated ability to assist and train others
12. Ability to work within a matrix model
13. International/ intercultural working skills
14. Open-minded to apply new digital solutions
Minimum Level of any Required Qualifications:
15. MD or eqivalent (DO, MBBS)
16. Specialization and training as a Rheumotologist
17. At least 4 years in pharmaceutical industry or CRO, previous experience in late stage clinical development
18. English fluent (spoken and written)
Why Choose Us?
19. Bring the miracles of science to life alongside a supportive, future-focused team.
20. Discover endless opportunities to grow your talent and drive your career, whether it’s through a promotion or a lateral move, at home or internationally.
21. Enjoy a thoughtful, well-crafted rewards package that recognizes your contribution and amplifies your impact.
22. 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 Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
#GD-SA
#LI-SA
#LI-Onsite
#vhd
Pursue, discover
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 and check out our Diversity Equity and Inclusion actions at !
Sanofi Inc. and its U.S. affiliates are Equal Opportunity and Affirmative Action employers committed to a culturally inclusive and diverse workforce. All qualified applicants will receive consideration for employment without regard to race; color; creed; religion; national origin; age; ancestry; nationality; natural or protective hairstyles; marital, domestic partnership or civil union status; sex, gender, gender identity or expression; affectional or sexual orientation; disability; veteran or military status or liability for military status; domestic violence victim status; atypical cellular or blood trait; genetic information (including the refusal to submit to genetic testing) or any other characteristic protected by law.
The salary range for this position is:
$236,250.00 - $393,750.00
All compensation will be determined commensurate with demonstrated experience. Employees may be eligible to participate in Company employee benefit programs. Additional benefits information can be found through the .