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Clinical Data Review Associate – Navi Mumbai, India

0-3 years
Not Disclosed
10 Nov. 19, 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

Clinical Data Review Associate – Navi Mumbai, India

Department: Data Management
Job ID: 11747
Work Model: Full-time, On-site

Overview

A leading global clinical research organization is seeking a Clinical Data Review Associate to join its Data Management team in Navi Mumbai. This role offers an excellent opportunity for professionals with a nursing background who want to build a long-term career in clinical data review and contribute to high-quality clinical research operations.

This position supports critical data review activities for clinical trials, ensuring accuracy, consistency, and compliance across global studies.

Key Responsibilities

  • Conduct detailed review of clinical trial data to ensure accuracy and protocol adherence.

  • Identify discrepancies and generate queries to resolve inconsistent or missing data.

  • Develop and maintain clinical data review guidelines and documentation.

  • Collaborate with cross-functional project teams to communicate data trends, findings, and quality insights.

Required Qualifications & Experience

  • Nursing degree (BSc Nursing or equivalent) is mandatory.

  • General understanding of clinical trial processes, GCP, and clinical data workflows.

  • Experience in clinical data review, clinical operations, or data management is preferred.

  • Entry-level candidates with strong academic background and interest in clinical research are encouraged to apply.

About the Organization

The employer is a globally recognized, full-service Clinical Research Organization (CRO) providing Phase I–IV clinical development services for biotechnology, pharmaceutical, and medical device companies. With headquarters in Cincinnati, Ohio, and operations in 40+ countries, the organization supports comprehensive clinical development through strong regulatory expertise and specialized therapeutic knowledge across oncology, cardiology, endocrinology, metabolic disorders, CNS, infectious diseases, and more.

Why Apply

This role offers:

  • Exposure to global clinical research projects

  • Structured career development in Data Management

  • A collaborative and growth-oriented work environment