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Associate – Evidence Synthesis- Clinical Outcome Assessments (Coa)

Sanofi
Sanofi
3+ years
preferred by company
10 Jan. 13, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate – Evidence Synthesis: Clinical Outcome Assessments (COA)

Location: Hyderabad, India
Employment Type: Full-Time, Permanent
Department: Clinical Outcome Assessments / Evidence Generation
Company: Sanofi


About Sanofi

Sanofi is a leading R&D-driven biopharmaceutical company, leveraging AI and digital innovation to improve patient outcomes worldwide. With a deep understanding of the immune system and a pioneering pipeline in immunology, chronic disease care, vaccines, and specialty medicines, Sanofi is committed to delivering breakthrough therapies that impact millions of lives globally.

The Sanofi Business Operations (SBO) hub in Hyderabad centralizes processes across Specialty Care, Vaccines, General Medicines, Consumer Health, Research & Development, and Data & Digital functions. SBO serves as a strategic partner to support Medical, Health Economics & Value Assessment (HEVA), Commercial, and R&D teams globally.


Role Overview

Sanofi is seeking an Associate – Evidence Synthesis (COA) to join the Global Clinical Outcome Assessment team in Hyderabad. The role focuses on generating robust patient-centered evidence to inform regulatory, clinical, and commercial decision-making. You will contribute to designing and validating Clinical Outcome Assessment (COA) instruments, performing evidence synthesis, and supporting strategic implementation of COA endpoints across clinical development programs.

This position offers a unique opportunity to work on innovative global healthcare projects, interact with cross-functional teams across time zones, and contribute to patient-focused drug development strategies.


Key Responsibilities

  • Execute assigned Evidence Synthesis projects, including search strategy development, literature screening, and data extraction, to generate high-quality clinical evidence

  • Support development and validation of COA instruments, including gap analyses, implementation, statistical analysis, and psychometric assessments

  • Prepare scientific documents such as reports, regulatory submissions, and publications in collaboration with senior team members

  • Contribute to COA endpoint strategies that enhance product value propositions for Global and Local markets

  • Translate qualitative and quantitative patient data into actionable insights for clinical and regulatory decision-making

  • Develop and maintain expertise in disease conceptual models, treatment paradigms, and evidence generation methodologies

  • Support stakeholder engagement with COA leads, HEVA, RWE, Clinical, Medical Affairs, Marketing, and Market Access teams globally

  • Contribute to process optimization, templates, and standardized approaches for COA evidence generation

  • Assist in preparing COA dossiers and supporting regulatory submissions (FDA, EMA, and other health authorities)

  • Maintain alignment with evidence generation guidelines and regulatory standards


Experience & Qualifications

Required:

  • Minimum 3+ years of experience in Clinical Outcome Assessments (COA) science, including COA data analysis, creation or validation of COA instruments, or implementation of COA endpoint strategies

  • Experience in pharmaceuticals, CROs, or academic research settings

  • Strong analytical skills to synthesize qualitative and quantitative evidence

  • Excellent stakeholder management, communication, and scientific writing skills

  • Ability to work independently and collaboratively in a global, cross-functional team environment

  • Exceptional proficiency in English (spoken and written)

Preferred:

  • Experience in regulatory COA submissions and dossier preparation

  • Familiarity with Health Economics & Outcomes Research (HEOR) or Patient-Reported Outcomes (PROs)

  • Understanding of COA instrument psychometrics, validation methods, and clinical trial integration


Why Join Sanofi Hyderabad

  • Be part of a global, innovative R&D organization driving patient-centered research

  • Work on a diverse portfolio, from established medicines to breakthrough therapies

  • Gain international exposure collaborating with teams across multiple time zones

  • Opportunity to develop career growth in evidence generation, COA science, and patient-centric research

  • Thrive in a diverse and inclusive workplace, committed to professional development


SEO & GEO Keywords

Clinical Outcome Assessment Jobs Hyderabad, COA Evidence Synthesis India, Patient-Reported Outcomes Careers, Sanofi Hyderabad Careers, Pharmaceutical Evidence Generation Jobs, COA Research Jobs