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

Medpace
Medpace
0-2 years
Not Disclosed
10 Dec. 29, 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 – Data Management

Location: Navi Mumbai, India
Employment Type: Full-Time, On-Site
Category: Clinical Data Management / Life Sciences
Experience Required: Entry-Level to Experienced Nurses
Job ID: 10929
Company: Medpace


Role Overview

Medpace is seeking a Clinical Data Review Associate to join our Data Management team in Navi Mumbai. This role provides an excellent opportunity for nurses to leverage their clinical knowledge while contributing to high-quality clinical trial data review. Both entry-level and experienced professionals are encouraged to apply.

As a Clinical Data Review Associate, you will play a critical role in ensuring accuracy, consistency, and compliance of clinical trial data, supporting the successful execution of studies across multiple therapeutic areas.


Key Responsibilities

  • Review clinical trial data to ensure accuracy, completeness, and compliance with protocols and regulatory requirements

  • Generate, manage, and resolve data queries to clarify inconsistencies or discrepancies

  • Assist in the development of clinical data review guidelines and SOPs

  • Collaborate with project teams to communicate review findings, trends, and data insights

  • Support the preparation of documentation for audits and inspections

  • Contribute to process improvement initiatives within the Data Management team


Required Qualifications

  • Nursing degree (B.Sc Nursing / equivalent)

  • General knowledge of clinical trial processes

  • Familiarity with clinical data collection, query management, and data validation

  • Strong attention to detail and ability to maintain high-quality standards

  • Effective written and verbal communication skills in English

  • Ability to work collaboratively in a team environment

Experience:

  • Entry-level applicants with a nursing degree are eligible

  • Experienced nurses with previous exposure to clinical trials or data management are highly encouraged to apply


About Medpace

Medpace is a full-service Contract Research Organization (CRO) delivering Phase I–IV clinical development services to biotechnology, pharmaceutical, and medical device industries globally. With over 30 years of experience and operations in more than 40 countries, Medpace accelerates the development of safe and effective medical therapeutics through a scientifically rigorous and disciplined approach.

Our therapeutic expertise spans oncology, cardiology, metabolic disease, endocrinology, central nervous system disorders, anti-viral and anti-infective therapies, among others.


Why Join Medpace?

  • Flexible and supportive work environment

  • Competitive compensation and benefits package

  • Generous paid time-off (PTO) and structured career paths

  • Opportunities for professional growth and learning

  • Employee wellness initiatives and company-sponsored appreciation events

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

  • Multiple CRO leadership awards from Life Science Leader Magazine for quality, reliability, and capability


Equal Opportunity Statement

Medpace is an equal opportunity employer committed to diversity, inclusion, and equitable treatment for all applicants.


Next Steps

Qualified candidates will be reviewed by a Medpace recruitment team. If selected, you will be contacted with detailed information about the interview process and next steps.