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Jr. Associate – Evidence Synthesis

1+ years
Not Disclosed
10 Nov. 21, 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

Jr. Associate – Evidence Synthesis | Hyderabad, India

Company: Sanofi
Job Type: Full-Time, Permanent
Experience Required: Minimum 1 year in HEOR (Health Economics and Outcomes Research) within pharmaceuticals, CRO, consulting, or academia


Job Overview

Sanofi is hiring a Jr. Associate – Evidence Synthesis to support global evidence generation initiatives across multiple therapeutic areas. This role contributes to the development of high-quality scientific and economic evidence that strengthens product value communication for global and local markets.

You will be part of Sanofi Business Operations (SBO), an internal global capability center based in India that supports Specialty Care, Vaccines, General Medicines, Consumer Healthcare, Contract Manufacturing, R&D, and Data & Digital functions. SBO delivers high-value services to global Medical, HEVA (Health Economics and Value Assessment), and Commercial teams.


Key Responsibilities

Evidence Synthesis & Research Support

  • Assist in executing Evidence Synthesis projects, including literature screening, data extraction, and full-text retrieval.

  • Support development of search strategies and contribute to evidence generation plans for pre-launch, launch, and post-launch products.

  • Work on studies such as burden of illness, epidemiology, literature reviews, meta-analyses, retrospective/ prospective observational studies, and economic evaluations.

  • Contribute to patient-reported outcomes research as required.

Therapeutic Area Expertise

  • Develop and maintain knowledge of assigned therapeutic areas to support evidence generation activities.

Performance & Delivery

  • Support the HEVA/Medical product leads in executing approved research studies.

  • Assist in managing ongoing studies to demonstrate clinical, economic, and humanistic value of products.

  • Facilitate coordination with institutions and external experts involved in evidence generation.

Process Development & Compliance

  • Assist in creating HEVA/Medical strategic evidence documents and scientific materials.

  • Support development of standardized templates, processes, and evidence generation tools aligned with global value communication requirements (e.g., CVD, AMCP dossiers).

  • Ensure compliance with internal evidence generation guidelines and scientific standards.

Stakeholder Collaboration

  • Support interactions with HEVA, Medical, RWE, Clinical, Market Access, Marketing, and External Affairs teams at regional and global levels.

  • Assist in developing tailored evidence deliverables required by cross-functional partners.

  • Ensure efficient communication and collaboration with global hub teams across time zones.


Required Qualifications

Experience

  • Minimum 1 year of experience in HEOR within:

    • Pharmaceutical industry

    • Contract Research Organization (CRO)

    • Consultancy

    • Academia

Education

  • Advanced degree in Life Sciences, Pharmacy, Medicine, Public Health, Biostatistics, Health Outcomes, or related field.

Skills

Soft Skills:

  • Strong communication and scientific writing skills

  • Stakeholder management

  • Ability to collaborate within cross-functional teams

  • Capacity to work independently

Technical Skills:

  • Analytical ability to interpret clinical and economic data

  • Understanding of evidence synthesis methodologies

  • Ability to contribute to payer-focused evidence strategies

Languages

  • Strong command of English (spoken and written)


Why Join Sanofi?

  • Opportunity to contribute to global scientific and value-driven initiatives.

  • Work in a future-focused environment that leverages AI and digital tools.

  • Access to professional development, training, and career mobility.

  • Competitive rewards and recognition programs.

  • Be part of a globally recognized biopharmaceutical leader committed to innovation and patient outcomes.


Equal Opportunity Commitment

Sanofi is an equal opportunity employer. The company does not discriminate based on race, colour, religion, sex, national origin, age, citizenship, marital status, disability, sexual orientation, gender identity, or any protected characteristic.