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Experienced Data Review Associate (Based In Pune)

2+ years
Not Disclosed
10 June 13, 2025
Job Description
Job Type: Full Time Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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 at Medpace – Pune (On-site)

Job Summary

Medpace, a globally recognized Clinical Research Organization (CRO), is hiring an Experienced Data Review Associate for its Pune office. This full-time role is ideal for candidates with a nursing or medical background, strong understanding of clinical data processes, and familiarity with MedDRA and WHO Drug dictionaries. Join a team dedicated to improving clinical trial quality across multiple therapeutic areas, including oncology and hematology.


Key Responsibilities

  • Conduct comprehensive manual reviews of clinical data collected in clinical trials.

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

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

  • Gain specialization in key therapeutic areas such as:

    • Oncology

    • Hematology

    • Infectious Diseases

    • Endocrinology

    • Metabolic Disorders


Required Skills & Qualifications

  • Bachelor’s Degree in Nursing/Medicine or a more advanced clinical qualification.

  • Professional or post-qualification nursing experience, preferably with an Oncology and Hematology background.

  • General understanding of clinical trial processes and handling clinical data.

  • Experience using MedDRA and WHO Drug dictionaries is a plus.


Perks & Benefits

  • Flexible work environment.

  • Competitive compensation and benefits package.

  • Generous PTO (Paid Time Off) programs.

  • Structured and clear career advancement pathways.

  • Participation in employee appreciation events.

  • Access to comprehensive health and wellness programs.

  • Opportunity to contribute to a globally awarded, industry-leading CRO.


Company Description

Medpace is a full-service global Clinical Research Organization (CRO) specializing in Phase I-IV clinical development for pharmaceutical, biotechnology, and medical device industries. The company leverages regulatory and therapeutic expertise in oncology, cardiology, metabolic disease, and more, ensuring superior clinical trial delivery worldwide.


Work Mode

On-site (Pune, India)


Call-to-Action

Are you ready to shape the future of clinical data management with a global CRO leader? Apply today and join Medpace’s dedicated team in delivering excellence in clinical research.