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Clinical Data Review Associate (Mumbai) - Entry/ Experienced Nurses Wanted

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

Clinical Data Review Associate – Nursing Graduates (Entry-Level & Experienced) | Medpace

Location: Navi Mumbai, India
Department: Clinical Data Management
Job ID: 10929
Employment Type: Full-Time, Office-Based

Role Overview

Medpace is expanding its clinical operations and is currently seeking a Clinical Data Review Associate to join the Data Management team at the Navi Mumbai office. This role is ideal for nursing graduates, both entry-level and experienced, who are looking to build a long-term career in clinical research and data management. The position offers structured professional development and the opportunity to contribute directly to global drug development projects.


Key Responsibilities

  • Review clinical trial data to ensure accuracy, completeness, and protocol compliance.

  • Identify, generate, and resolve data queries to address inconsistencies and improve data quality.

  • Contribute to the development of clinical data review guidelines and study-specific processes.

  • Collaborate with project teams to communicate data trends, clarify findings, and support overall study execution.


Required Qualifications

  • Bachelor’s degree in Nursing (B.Sc Nursing / GNM / equivalent).

  • General understanding of clinical trial processes or prior experience with clinical data is preferred.

  • Both fresh graduates and experienced nursing professionals are encouraged to apply.

  • Strong analytical thinking and attention to detail.

  • Ability to work in a fast-paced, team-oriented environment.


About Medpace

Medpace is a full-service global Clinical Research Organization (CRO) supporting Phase I–IV clinical trials across biotechnology, pharmaceutical, and medical device sectors. With headquarters in Cincinnati, Ohio, and operations in more than 40 countries, Medpace is recognized for its scientific excellence, regulatory expertise, and commitment to accelerating the development of safe and effective therapeutics.

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


Why Join Medpace

  • Flexible work environment.

  • Competitive compensation and benefits.

  • Attractive paid time off (PTO) structure.

  • Clear career progression and continuous learning opportunities.

  • Employee wellness initiatives and appreciation events.

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

  • Multiple CRO Leadership Awards for quality, capability, and performance.


Next Steps

Once you apply, a Medpace recruitment team member will review your profile. If shortlisted, you will be contacted for the next steps in the hiring process.