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Experienced Data Review Associate (Pune)

0-2 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

Experienced Data Review Associate – Pune, India

Department: Data Management
Job ID: 11330
Location: Pune, India

Job Overview

Medpace, a leading global Clinical Research Organization (CRO), is expanding its operations and is seeking an Experienced Data Review Associate to join the Global Clinical Coding & Support team in Pune. This full-time position is ideal for professionals with a nursing or clinical background who want to advance their career in clinical data review within a structured, growth-focused environment.

As part of the Data Management function, you will support key clinical programs by ensuring the accuracy, consistency, and integrity of clinical trial data across therapeutic areas.


Key Responsibilities

  • Perform comprehensive manual review of clinical data collected during clinical trials.

  • Develop clinical data review guidelines tailored to specific therapeutic areas.

  • Collaborate with the Data Management team to drive efficient query resolution.

  • Contribute expertise in specialized clinical domains including:

    • Oncology

    • Hematology

    • Infectious Diseases

    • Endocrinology

    • Metabolic Disorders


Required Qualifications and Experience

  • Bachelor’s degree in Nursing, Medicine, or an advanced clinical qualification.

  • Professional or post-qualification nursing experience, preferably in Oncology or Hematology.

  • Solid understanding of clinical trial processes and experience working with clinical data.

  • Familiarity with MedDRA and WHO Drug Dictionary is an added advantage.

This role is suited for candidates with existing experience in clinical data review or nursing professionals looking to transition into clinical data management.


About Medpace

Medpace is a full-service global CRO providing Phase I–IV clinical development services for pharmaceutical, biotechnology, and medical device organizations. With headquarters in Cincinnati, Ohio, and operations in more than 40 countries, Medpace integrates scientific expertise, regulatory knowledge, and operational excellence to accelerate the development of safe and effective medical therapies.

Therapeutic expertise includes oncology, cardiology, metabolic diseases, endocrinology, CNS, antiviral, and infectious diseases.


Why Join Medpace

Medpace offers a career environment rooted in purpose, scientific discipline, and global impact. Over the past three decades, Medpace has contributed to breakthroughs that have shaped modern clinical development.

Benefits include:

  • Flexible working environment

  • Competitive salary and benefits

  • Generous PTO plans

  • Clear, structured career paths and advancement opportunities

  • Company-sponsored recognition and appreciation programs

  • Employee health and wellness initiatives

Recognition:

  • Listed by Forbes as one of America’s Most Successful Midsize Companies (2021–2024)

  • Multiple CRO Leadership Awards from Life Science Leader for expertise, reliability, quality, and capability


What to Expect Next

Once your application is submitted, the Medpace recruitment team will review your qualifications. If your profile aligns with the role, you will be contacted with next steps in the selection process.