Senior Clinical Scientist

Sanofi

Senior Clinical Scientist on the Rheumatology/Transplant Clinical Development Team at Sanofi. Providing medical and scientific support throughout clinical trial setup to report completion.

Posted 7/3/2026full-timeCambridge • Massachusetts, New Jersey • 🇺🇸 United StatesSenior💰 $148,500 - $214,500 per yearWebsite

About the role

Key responsibilities & impact

Support the design and execution of multiple clinical studies across the development plan
Help prepare key trial documents — protocols, informed consent forms, and benefit-risk assessments
Contribute to CRF design and review completion instructions
Support study start-up, site opening, and enrollment monitoring
Review and analyze data listings, patient profiles, and key study data within statistical reports
Partner with Data Management to generate relevant queries
Stay current on competitive data and the therapeutic landscape
Deliver clinical landscape and benchmark updates to the CRD and Project Lead
Partner with Clinical Leads and CRDs to build presentations for governance committees
Serve as delegate for the CRD in developing and overseeing the clinical development plan
Act as liaison across data management, biostatistics, medical writing, pharmacovigilance, regulatory affairs, clinical operations, and translational medicine
Support project team members, project management, and medical affairs
Co-author briefing packages for health authority submissions and contribute to regulatory strategy
Build and maintain relationships with internal collaborators, KOLs, and investigators
Support interactions with Sanofi governance bodies, external partners, and committees

Requirements

What you’ll need

PharmD or PhD holders: minimum 4 years of clinical development experience
Master's degree holders: minimum 7 years of clinical development experience
Late-stage clinical development experience (Phase 2b/3 preferred)
Rheumatology or immunology therapeutic area background
Hands-on experience with clinical trial preparation and execution
Knowledge of translational medicine and biomarkers
Strong statistical and data analysis skills
Proven track record managing complex global projects
Experience leading cross-functional teams
Excellent communication and problem-solving abilities
Regulatory authority interaction experience

Benefits

Comp & perks

high-quality healthcare
prevention and wellness programs
at least 14 weeks’ gender-neutral parental leave

ATS Keywords

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Applicant Tracking System Keywords

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Hard Skills & Tools

Clinical DevelopmentStatistical AnalysisData AnalysisClinical Trial PreparationCRF DesignRegulatory StrategyBenefit-Risk AssessmentTranslational MedicineBiomarkersProject Management

Soft Skills

Excellent CommunicationProblem-Solving Abilities

Certifications

PharmDPhD