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Rwe Scientist

7 years
Not Disclosed
10 Feb. 11, 2025
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

Job Title: RWE Scientist

Location: Hyderabad, India
Department: Sanofi Business Operations – Scientific Communications
Job Type: Permanent, Full-time
Reporting to: Head of Scientific Communications, Sanofi Business Operations
Travel Requirement: As per business needs


ABOUT THE COMPANY

Sanofi Business Operations is an internal strategic and functional partner supporting Specialty Care, Vaccines, General Medicines, CHC, CMO, and R&D, Data & Digital functions globally. The organization aims to centralize processes for enhanced efficiency in Medical, HEVA, and Commercial functions worldwide.


JOB SUMMARY

The Real-World Evidence (RWE) Scientist will play a critical role in developing and executing evidence strategies for drug development and enablement projects at a global level. The role involves collaborating with cross-functional teams to ensure scientifically rigorous, timely, and cost-effective real-world studies that meet business and regulatory requirements.


KEY RESPONSIBILITIES

Strategic RWE Development & Execution

  • Support RWE Strategy Leads in the design, execution, analysis, interpretation, and communication of epidemiological/outcomes research studies.
  • Provide strategic input to maximize market potential, manage risks, and optimize research methodologies.
  • Develop real-world evidence strategies to support regulatory submissions, drug discovery, development, and commercialization.
  • Identify and validate fit-for-purpose external data sources and institutions in collaboration with RWD&ES teams.
  • Ensure scientific rigor, ethical integrity, and business relevance in all study executions.

Data Utilization & Methodological Innovation

  • Set standards for real-world evidence utilization and provide methodological leadership.
  • Apply innovative RWE methodologies to address evidence gaps and support product lifecycle management.
  • Work with routinely collected data (claims databases, EMRs, registries, structured/unstructured healthcare sources).
  • Translate business needs into study and data requirements for optimized research execution.

Project & Stakeholder Management

  • Oversee end-to-end execution of real-world studies to ensure timely, budget-friendly, and high-quality deliverables.
  • Collaborate with internal teams and external stakeholders to mitigate risks, optimize resources, and drive efficiency.
  • Maintain transparent communication with global stakeholders regarding project progress, challenges, and key insights.
  • Provide scientific support and expertise in a specific epidemiological area and therapy area.

QUALIFICATIONS & EXPERIENCE

Education:

  • Advanced degree (Ph.D., M.Sc., or equivalent) in Pharmacoepidemiology, Biostatistics, Health Outcomes, or related fields.

Experience:

  • 7+ years of experience in real-world evidence generation within the pharmaceutical industry.
  • Expertise in RWE application for drug development, regulatory approval, and patient access.
  • Strong knowledge of product lifecycle processes and innovative RWE methodologies.
  • Experience across multiple therapeutic areas, with a preference for transplant, diabetes (Type 1/2), and cardiovascular diseases.
  • Cross-functional collaboration experience in complex global matrix teams.

SKILLS & COMPETENCIES

Soft Skills:

  • Excellent written and verbal communication, negotiation, and interpersonal skills.
  • Proven teamwork and collaboration skills in a global, multicultural environment.
  • Strong sense of urgency, ownership, and proactive problem-solving.
  • Ability to adapt communication for diverse audiences (scientific, commercial, and executive stakeholders).
  • Growth mindset with a proactive approach to learning and skill development.

Technical Skills:

  • Expertise in Pharmacoepidemiology, HEOR, and RWE study designs & methodologies.
  • Experience with real-world data (claims databases, EMRs, registries, structured/unstructured healthcare sources).
  • Strong project management skills for real-world studies and reporting.

Languages:

  • Fluency in English (spoken and written) is mandatory.
  • Proficiency in French or other European languages is a plus.

WHY JOIN SANOFI?

At Sanofi, we believe in making a real impact through innovation, collaboration, and excellence. We provide a diverse, inclusive, and dynamic work environment where employees can grow and thrive.

"Better is out there. Better medications, better outcomes, better science. But progress doesn’t happen without people. Let’s make miracles happen together."