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Associate Director Real World Evidence

5-8 years
Not Disclosed
10 Nov. 6, 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

Associate Director – Real World Evidence

Job ID: 292004
Location: Bangalore, Karnataka, India
Job Type: Full-time


About the Company

Work Your Magic with Us!
We are innovators driven by curiosity, science, and technology—committed to enriching people’s lives across Healthcare, Life Science, and Electronics. Our teams collaborate globally to push boundaries, explore new possibilities, and create real-world impact for patients, customers, and communities.

In our Healthcare division, united as one for patients, our mission is to help create, improve, and prolong lives. We develop medicines, intelligent devices, and innovative technologies in key therapeutic areas such as Oncology, Neurology, and Fertility.
Joining our team means becoming part of a diverse, inclusive, and flexible work culture that promotes personal growth and global career advancement.


Role Overview

We are seeking an Associate Director – Real World Evidence (RWE) to join our Global Oncology RWE team.
Reporting to the Global Head of Real World Evidence (Oncology), this role will shape and implement RWE strategies that enhance data-driven decision-making and value creation across oncology programs.


Key Responsibilities

As the Associate Director, Real World Evidence, you will:

  • Serve as the functional product lead and subject matter expert (SME) for assigned products.

  • Lead the RWE strategy as part of the Integrated Evidence Plan (IEP) for oncology products.

  • Execute and manage RWE projects across multiple data sources and geographies.

  • Identify and select fit-for-purpose real-world data (RWD) sources aligned to key research questions.

  • Act as study lead for Non-Interventional Studies (NIS).

  • Lead cross-functional analysis requests and ensure timely, high-quality output.

  • Provide scientific input in product team meetings and strategic discussions (e.g., benefit-risk assessments, clinical sub-teams, publication strategy).

  • Develop epidemiology sections for submission documents such as Risk Management Plans (RMPs), DSURs, and other regulatory filings.

  • Support regulatory agency interactions by preparing responses and attending Health Authority (HA) meetings.

  • Contribute to publications, study proposals, and expert reviews from internal and external stakeholders.

  • Lead Business Plan initiatives, ensuring strategic implementation and measurable impact.

  • Promote strong communication and collaboration across stakeholders.

  • Drive process improvements and apply lean concepts for simplification and efficiency.

  • Implement scientific best practices across the RWE function and broader organization.

  • Mentor and develop junior RWE scientists, fostering continuous learning and growth.


Who You Are

  • Education: Master’s or Doctoral degree (PhD) in (pharmaco)epidemiology, public health, or biostatistics.

  • Language: Fluent in Business English (written and spoken).

  • Experience:

    • 5–8 years of experience in (pharmaco)epidemiology within the pharmaceutical, biotechnology, CRO, or academic settings.

    • Proven expertise in RWD and RWE studies design, execution, and interpretation.

    • Strong background in epidemiologic methodologies, data analysis, and project management.

    • Exposure to global, cross-functional environments and multicultural teams.

    • Sound understanding of drug development processes, and the interfaces between clinical development, regulatory, and commercial functions.

    • Experience in global regulatory or payer submissions and interactions.

    • Familiarity with regulatory frameworks and standards such as GPP, GVP, and ENCePP.

    • Knowledge of medical, pharmacological, and pharmacovigilance principles is a plus.


What We Offer

We are curious minds from diverse backgrounds, united by innovation and driven by impact.
We believe that diversity fosters excellence and innovation—strengthening our ability to lead in science and technology.

Our culture offers:

  • Inclusive and supportive environment

  • Opportunities for professional development and global growth

  • Empowerment to explore and innovate at your own pace

Join us in building a workplace that sparks discovery, elevates humanity, and champions human progress.

Apply now and be part of a team dedicated to advancing healthcare through Real World Evidence.

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