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 Requirements 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 #J-18808-Ljbffr