Senior Clinical Scientist

Responsibilities

• 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

• 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