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Associate Director Real World Evidence

5-8 years
Not Disclosed
10 Nov. 27, 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

Associate Director – Real World Evidence (RWE)

Job ID: 292004 | Bangalore, Karnataka, India | Full-Time

Position Overview

The Associate Director, Real World Evidence (RWE), will play a strategic leadership role within the global Oncology RWE function. Reporting to the Global Head of Real World Evidence Oncology, this position is responsible for shaping and driving RWE strategies that enhance scientific decision-making, regulatory readiness, and value demonstration across the oncology portfolio.

This role requires deep expertise in pharmacoepidemiology, real-world data (RWD) methodologies, and execution of global non-interventional research programs.


Key Responsibilities

RWE Strategy & Leadership

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

  • Lead the RWE strategy as part of the Integrated Evidence Plan (IEP) and ensure alignment with clinical, medical, safety, and market access goals.

  • Drive end-to-end execution of the RWE strategy for assigned products.

Real-World Data & Study Execution

  • Identify, evaluate, and recommend fit-for-purpose RWD sources globally, ensuring relevance for specific research questions.

  • Act as Study Lead for Non-Interventional Studies (NIS), overseeing design, execution, quality, and reporting.

  • Lead cross-functional analysis requests and ensure timely, scientifically sound outputs.

Regulatory & Scientific Contributions

  • Provide epidemiological content for regulatory submissions including RMPs, DSURs, and other safety/clinical documentation.

  • Support interactions with Health Authorities, including development of responses and participation in meetings.

  • Contribute to peer-reviewed publications, expert reviews, and internal scientific assessments.

Cross-Functional Collaboration

  • Actively participate in product team meetings, benefit-risk discussions, publication strategy forums, and other strategic working groups.

  • Ensure alignment across internal stakeholders, promoting efficient communication and transparent information flow.

Process Excellence & Organizational Development

  • Lead process improvement initiatives using lean methodologies, promoting simplification and efficiency.

  • Contribute to the implementation of scientific best practices across the RWE organization.

  • Mentor and support junior RWE scientists, fostering capability development and scientific rigor.


Candidate Profile

Education

  • Master’s degree or Doctoral degree (PhD) in Pharmacoepidemiology, Epidemiology, Public Health, Biostatistics, or related fields.

Experience Requirements

  • 5–8 years of experience in pharmacoepidemiology or RWE roles within the Pharmaceutical or Biotechnology industry, academic research settings, or CROs.

  • Demonstrated experience conducting studies using real-world data sources (claims, EMR, registries, etc.).

  • Strong foundations in epidemiologic study design, RWD analytics, and interpretation of observational research.

  • Experience managing full study life cycles in a global or multi-cultural environment.

  • Solid understanding of drug development processes and cross-functional interdependencies.

  • Experience with global regulatory and payer submissions, including familiarity with GPP, GVP, ENCePP standards.

Skills & Competencies

  • Strong analytical skills and scientific leadership capabilities.

  • Excellent communication skills in business-level English.

  • Ability to lead cross-functional initiatives and influence strategic decisions.

  • Proven ability to manage multiple projects and deliver high-quality scientific outputs.


What We Offer

We offer a diverse, inclusive, and globally connected working environment that thrives on scientific innovation and collaboration. Our culture encourages continuous learning, personal growth, and professional advancement. You will be part of a global healthcare organization committed to improving lives, advancing science, and shaping the future of Real-World Evidence in oncology.


Apply Now

If you are driven by scientific excellence, real-world data innovation, and global healthcare impact, apply today and join a team dedicated to advancing evidence generation and improving patient outcomes.