Associate Position in Evidence Synthesis (Clinical Outcome Assessments) at Sanofi – Life Sciences, Pharmacy, Public Health, Psychology, Biostatistics Sanofi in

Sanofi, a global leader in R&D-driven biopharmaceuticals, is hiring for the position of Associate – Evidence Synthesis (Clinical Outcome Assessments) at its Hyderabad, India location. This full-time, permanent role is part of Sanofi Business Operations and supports global research and development initiatives focused on patient-centric outcomes and evidence-based decision-making. The position is ideal for professionals with experience in COA science, evidence synthesis, qualitative and quantitative research, and regulatory-focused documentation, seeking to advance their career in a global biopharma environment.

Key responsibilities include executing evidence synthesis projects, developing disease conceptual models and COA landscape analyses, supporting the selection, development, validation, and psychometric assessment of COA instruments, conducting qualitative and quantitative research (including patient experience and preference studies), and assisting in the preparation of COA dossiers, briefing books, regulatory submissions, and scientific publications. The role involves collaboration with global stakeholders across COA, HEVA, RWE, Clinical, Medical Affairs, Market Access, and Regulatory teams, and contributing to COA endpoint strategies aligned with best-in-class product approaches. Adherence to FDA, EMA, and global evidence-generation guidelines is required.

Applicants should have a Master’s degree (preferred) in Life Sciences, Pharmacy, Public Health, Psychology, Biostatistics, or a related discipline, with at least 3 years of experience in clinical outcome assessments, evidence synthesis, COA data analysis, and development or validation of COA instruments. Experience in the pharmaceutical industry, CRO, consultancy, or academia is expected. Key skills include strong analytical and scientific writing abilities, experience with patient-reported outcomes and psychometric validation, excellent stakeholder management, cross-functional collaboration, and exceptional English communication skills.

The estimated salary range is ₹10,00,000 – ₹18,00,000 per annum (CTC), with competitive compensation, exposure to global R&D projects, career growth opportunities, and an inclusive, diverse workplace culture. The deadline to apply is February 10, 2026. Interested candidates should apply online via the provided application link, ensuring their CV and supporting documents highlight relevant experience and qualifications.

Relevant academic keywords include Evidence Synthesis, Clinical Outcome Assessments, Life Sciences, Pharmacy, Public Health, Psychology, Biostatistics, Health Economics, Value Assessment, HEVA, HEOR, Patient-Reported Outcomes, and Regulatory Science. This opportunity is ideal for those seeking to influence regulatory and reimbursement decision-making, drive patient-focused clinical research, and build a long-term career within a top-tier biopharmaceutical organization.