Associate – Evidence Synthesis: Clinical Outcome Assessments (COA)
Location: Hyderabad, India
Job Type: Full-Time, Permanent
About Sanofi
Sanofi is a global, R&D-driven biopharma company, committed to improving lives through innovative medicines and vaccines. Leveraging AI-powered technology and patient-centric approaches, Sanofi addresses chronic diseases, immunology, diabetes, and transplant complications, aiming to maximize patient outcomes worldwide.
Sanofi Business Operations (SBO), based in India, centralizes processes to support Specialty Care, Vaccines, General Medicines, Consumer Healthcare, Research & Development, and Data & Digital functions, acting as a strategic partner to global and local teams.
Role Overview
The Associate – Evidence Synthesis (COA) will contribute to evidence generation and clinical outcome assessment strategies for Sanofi’s global R&D projects. This role focuses on incorporating patient perspectives into clinical research through Clinical Outcome Assessments (COAs), supporting regulatory submissions, and driving strategic decision-making.
Key Responsibilities
Execute assigned Evidence Synthesis projects, including search strategy development, screening, and data extraction.
Support disease and treatment paradigm research through primary and secondary research.
Generate evidence to support the development or use of Fit-for-Purpose COA instruments, including gap analyses, psychometric validation, statistical analyses, and dissemination.
Prepare scientific documentation (reports, regulatory submissions, publications) in collaboration with senior team members.
Contribute to the COA endpoint strategy, aligned with Sanofi’s Best-in-Class and First-in-Class approach.
Collaborate with global COA leads, HEVA, RWE, Clinical, Medical Affairs, Marketing, and Market Access teams to identify evidence needs and support deliverables.
Maintain adherence to regulatory guidelines (FDA, EMA) and evidence generation standards.
Support development of COA dossiers and provide input on evidence generation strategy.
Qualifications & Experience
Essential:
Bachelor’s or Master’s degree in Pharmaceutical Sciences, Life Sciences, or related field.
Minimum 3 years of experience in COA science, including data analyses, instrument validation, or endpoint strategy implementation.
Strong analytical skills to synthesize qualitative and quantitative data.
Proven ability to work independently and collaboratively within cross-functional teams.
Exceptional English communication skills (written and spoken).
Preferred:
Experience in pharmaceutical industry, CRO consultancy, or academia with COA-related projects.
Familiarity with regulatory documentation and submissions involving patient-reported outcomes.
Why Join Sanofi
Work with innovative, global teams driving breakthroughs in patient-centered healthcare.
Opportunity to grow professionally through mentorship and exposure to complex evidence generation projects.
Contribute to patient-focused strategies that influence regulatory and reimbursement decisions globally.
Be part of a diverse and inclusive workplace, committed to equal opportunities and career development.
Sanofi is an equal opportunity employer, committed to diversity, equity, and inclusion across all aspects of employment.
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