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Associate - Evidence Synthesis

3+ years
Not Disclosed
10 Oct. 27, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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

Job Title: Associate – Evidence Synthesis

📍 Location: Hyderabad, India
🕒 Job Type: Permanent | Full-time
🧳 Travel: As per business need
👤 Hiring Manager: Head / Group Lead / Team Lead
🏢 Department: Sanofi Business Operations (SBO)


About Sanofi

At Sanofi, you’ll break new ground across a diverse and growing portfolio — from established medicines relied on by millions to pioneering breakthroughs in immunology and chronic disease care.
Fueled by advances in technology, Sanofi is accelerating innovation and expanding access faster than ever. Join us where ambition meets impact, powered by AI and digital transformation.


About the Team

Sanofi Business Operations (SBO) is an internal resource organization based in India. It centralizes processes to support global functions such as:

  • Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, and Data & Digital functions.
    SBO serves as a strategic partner for tactical deliveries to Medical, Health Economics and Value Assessment (HEVA), and Commercial organizations across Sanofi globally.


Main Responsibilities

Core Purpose

Contribute to the execution of Evidence Synthesis projects (e.g., search strategy development, screening, data extraction) to generate robust scientific evidence supporting Sanofi’s global and local programs.

Key Duties

  • Support HEVA and Medical teams in evidence generation, analysis, and dissemination across the product lifecycle (pre-launch, launch, and post-launch).

  • Contribute to studies on epidemiology, burden of illness, meta-analysis, retrospective/prospective studies, economic evaluations, and patient-reported outcomes.

  • Assist in the creation and updating of Core Value Dossiers (CVDs) and AMCP dossiers to inform payer and access strategies.

  • Develop and maintain therapeutic area (TA) expertise.

  • Support adherence to publication and evidence generation standards.

  • Collaborate with global and regional stakeholders across HEVA, RWE, Medical Affairs, Market Access, and Commercial teams.


People Responsibilities

  • Build and maintain effective relationships with global HEVA and Medical teams across time zones.

  • Work collaboratively with internal teams to ensure smooth delivery of assigned projects.


Performance Responsibilities

  • Execute assigned evidence synthesis activities with scientific accuracy and timeliness.

  • Support ongoing HEVA/Medical studies to demonstrate clinical, economic, and humanistic value.

  • Contribute to the generation and presentation of scientific evidence supporting access and reimbursement decisions.


Process Responsibilities

  • Support the development and optimization of evidence generation processes, templates, and materials.

  • Ensure adherence to global evidence generation standards and compliance guidelines.

  • Assist in innovation initiatives to improve evidence identification and communication strategies.


Stakeholder Management

  • Collaborate with cross-functional teams including HEVA, RWE, Clinical, Medical Affairs, Marketing, External Affairs, and Market Access.

  • Contribute to customized evidence deliverables for internal and external stakeholders.


About You

🎓 Education:

  • Advanced degree in Life Sciences, Pharmacy, or a related medical/scientific discipline.

💼 Experience:

  • Minimum 3+ years in Health Economics and Outcomes Research (HEOR) within the pharmaceutical industry, CRO, or academia.

🧠 Technical Skills:

  • Strong analytical and critical appraisal skills.

  • Ability to translate complex clinical and economic data into payer-relevant insights.

  • Familiarity with systematic review methodologies and evidence synthesis tools.

💬 Soft Skills:

  • Excellent communication and writing abilities.

  • Strong stakeholder management and teamwork capabilities.

  • Self-motivated with the ability to work independently.

🌐 Languages:

  • Excellent command of English (spoken and written).