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Jr. Associate – Evidence Synthesis

1+ years
Not Disclosed
10 Nov. 10, 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: Jr. Associate – Evidence Synthesis
Company: Sanofi
Location: Hyderabad, India
Job Type: Permanent, Full-time
Travel Requirement: As per business needs


Team / Department Overview:

  • Role is part of Sanofi Business Operations (SBO), an internal resource organization in India.

  • SBO centralizes processes and activities to support Specialty Care, Vaccines, General Medicines, CHC, CMO, R&D, Data & Digital functions.

  • SBO partners with Medical, Health Economics and Value Assessment (HEVA), and Commercial teams globally to deliver evidence-based insights.


Role Summary:

Assist in the execution of evidence synthesis projects to generate robust clinical, economic, and humanistic evidence supporting Sanofi programs/products for global and local markets. Develop therapeutic area expertise and contribute to strategic evidence generation processes.


Key Responsibilities:

1. Evidence Generation & Analysis:

  • Assist in the execution of evidence synthesis projects, including:

    • Search strategy development

    • Screening and data extraction

    • Full-text downloading

  • Support research plans for pre-launch, launch, and post-launch evidence.

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

2. Study Execution & Management:

  • Support approved HEVA/Medical studies and manage ongoing studies if required.

  • Assist HEVA/Medical product leads in executing studies that demonstrate clinical, economic, and humanistic product value.

3. Process & Documentation:

  • Assist in developing core HEVA/Medical strategic evidence materials and templates.

  • Maintain adherence to evidence generation guidelines and standards.

4. Stakeholder Engagement:

  • Support internal engagement with HEVA, Medical, RWE, Clinical, Medical Affairs, Marketing, External Affairs, and Market Access teams.

  • Prepare relevant deliverables tailored to internal and external stakeholders.


Qualifications & Experience:

  • Education: Advanced degree in life sciences, pharmacy, or medical discipline (or equivalent).

  • Experience: 1+ years in Health Economics and Outcomes Research (HEOR) within the pharmaceutical industry, CRO consultancy, or academia.

  • Technical Skills: Strong analytical skills to translate clinical and economic information into evidence strategies.

  • Soft Skills:

    • Stakeholder management

    • Effective written and verbal communication

    • Ability to work independently and collaboratively


Languages:

  • Excellent English proficiency (spoken and written)


Why Sanofi:

  • Work on a growing, diverse portfolio including immunology, chronic disease, diabetes, cardiovascular disease, and transplant care.

  • Opportunity to leverage AI and digital tools to accelerate healthcare innovation.

  • Inclusive work environment with equal opportunities for all employees.

  • Commitment to professional growth and transformative career experiences.