Senior Associate – Evidence Synthesis (Clinical Outcome Assessments – COA)
Location: Hyderabad, India
Job Type: Permanent | Full-Time
Travel: As per business requirements
Experience Level: Senior / Mid–Senior
Experience Required: Minimum 5+ Years
Function: Evidence Synthesis | Clinical Outcome Assessments
Reporting To: Head / Group Lead / Team Lead / Manager
Job Overview
Sanofi is seeking a highly skilled Senior Associate – Evidence Synthesis (Clinical Outcome Assessments) to join its growing team in Hyderabad. This role is pivotal in integrating the patient perspective into clinical research by generating high-quality COA evidence to support regulatory, reimbursement, and strategic decision-making across global and local markets.
The position offers an opportunity to work at the intersection of science, patient-centric research, and innovation within a global, R&D-driven, AI-powered biopharmaceutical organization.
About Sanofi
Sanofi is a global healthcare leader committed to improving lives through innovative medicines and vaccines. With deep expertise in immunology and chronic disease care, Sanofi leverages advanced technology and data-driven insights to accelerate innovation and expand patient access worldwide.
Sanofi Business Operations (SBO), based in India, serves as a strategic internal partner supporting Medical, HEVA, Commercial, R&D, and Digital functions across global operations.
Role Summary
The Clinical Outcome Assessments (COA) team operates within Sanofi’s Global R&D under the Patient-Informed Development & Health Value Translation (PID & HVT) function. The Evidence Synthesis team in Hyderabad supports global COA evidence generation, enabling robust patient-centric outcome strategies aligned with regulatory expectations (FDA, EMA) and value demonstration.
Key Responsibilities
Evidence Synthesis & COA Strategy
Execute evidence synthesis activities including literature search strategy development, screening, and data extraction
Develop a comprehensive understanding of disease areas and treatment paradigms using primary and secondary research
Independently generate evidence supporting fit-for-purpose COA instrument selection, development, and validation
Conduct gap analyses, psychometric validation, statistical analyses, and COA implementation planning
Contribute to optimized COA endpoint strategies aligned with Best-in-Class / First-in-Class product development
Scientific & Regulatory Deliverables
Prepare high-quality scientific documents including reports, regulatory dossiers, briefing books, and publications
Support development of COA dossiers and provide strategic input for regulatory submissions
Contribute to Target Value Propositions with patient-centric outcome messaging
Cross-Functional Collaboration
Act as a subject matter expert (SME) to guide team members on evidence synthesis and COA execution
Collaborate with global COA leads across multiple time zones
Work closely with HEVA, RWE, Clinical, Medical Affairs, Market Access, Marketing, and External Affairs teams
Support customized deliverables aligned with stakeholder evidence needs
Process & Innovation
Contribute to development and standardization of COA evidence generation processes, templates, and best practices
Ensure compliance with internal standards and global evidence generation guidelines
Identify opportunities to innovate COA evidence generation and dissemination to enhance regulatory and reimbursement impact
Required Qualifications & Skills
Education
Master’s or Bachelor’s degree in Life Sciences, Public Health, Psychology, Health Outcomes Research, or a related discipline
Experience
Minimum 5+ years of experience in COA science, evidence synthesis, or outcomes research
Hands-on experience in COA data analysis, development, validation, or endpoint strategy within pharma, CRO, consultancy, or academia
Technical Skills
Strong analytical skills to synthesize qualitative and quantitative data
Expertise in translating COA data into evidence strategies and value messages
Experience with literature reviews, qualitative research, and psychometric validation
Soft Skills
Excellent stakeholder management and collaboration skills
Strong scientific writing and communication abilities
Ability to work independently while leading and delivering complex projects
Language
Exceptional proficiency in English (written and spoken)
Why Join Sanofi
Work on global, patient-centric clinical development programs
Collaborate with cross-functional and international teams
Leverage AI, digital tools, and innovative methodologies
Access continuous learning, career growth, and development opportunities
Be part of a purpose-driven organization improving lives worldwide
Equal Opportunity Statement
Sanofi is an equal opportunity employer and is committed to fostering diversity, equity, and inclusion across all levels of the organization. Employment decisions are based on merit, qualifications, and business needs.
Apply now on thepharmadaily.com and be part of a global organization where science, innovation, and patient outcomes come together to shape the future of healthcare.
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