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

Medpace
Medpace
0-2+ years
preferred by company
10 Jan. 14, 2026
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

Location: Navi Mumbai, India
Department: Data Management
Employment Type: Full-Time | Office-Based
Job ID: 12326
Company: Medpace

About the Role

Medpace, a leading global full-service Contract Research Organization (CRO), is expanding its Data Management team in Mumbai, India. We are seeking Clinical Data Review Associates with a nursing background—both entry-level and experienced professionals are encouraged to apply. This role offers the opportunity to leverage your nursing expertise, gain hands-on experience with clinical trial data, and develop a rewarding career in clinical research.

As a Clinical Data Review Associate, you will play a critical role in ensuring the accuracy, quality, and integrity of clinical trial data that supports the development of innovative therapies across multiple therapeutic areas.

Key Responsibilities

  • Review clinical trial data for accuracy, completeness, and compliance with study protocols.

  • Identify, generate, and resolve data queries to clarify discrepancies or inconsistencies.

  • Develop and apply clinical data review guidelines to maintain standardization and quality.

  • Collaborate and communicate with cross-functional project teams to discuss review findings, trends, and data-related recommendations.

  • Support continuous improvement initiatives within data management processes.

Required Qualifications and Experience

  • Nursing degree (B.Sc Nursing, GNM, or equivalent).

  • General knowledge of clinical trial processes and regulatory requirements.

  • Experience working with clinical data is preferred but not mandatory; both freshers and experienced nurses are encouraged to apply.

  • Strong analytical skills, attention to detail, and ability to work in a team-oriented environment.

  • Excellent written and verbal communication skills.

Why Medpace?

Medpace is a global leader in Phase I-IV clinical research, partnering with biotechnology, pharmaceutical, and medical device companies worldwide. With a presence in 40+ countries and over 5,000 employees, we offer structured career paths, mentorship opportunities, and a collaborative work environment where your contributions make a direct impact on patient care and clinical research.

Employee Benefits and Perks:

  • Flexible office and hybrid work arrangements

  • Competitive compensation and benefits

  • Paid time off and leave entitlements

  • Career development programs and structured growth opportunities

  • Company-sponsored employee engagement and wellness initiatives

  • Recognized globally for excellence in CRO services and leadership

Awards and Recognition:

  • Forbes: America's Most Successful Midsize Companies (2021–2024)

  • Life Science Leader CRO Leadership Awards (CRO2024)

About Medpace

Medpace is dedicated to accelerating the global development of safe and effective medical treatments across key therapeutic areas including oncology, cardiology, metabolic diseases, CNS, anti-infectives, and more. With over 30 years of expertise, our scientific approach and disciplined methodology help improve the lives of patients worldwide.


Apply Today – Take the next step in your clinical research career. Both entry-level and experienced nurses are encouraged to join Medpace and contribute to global clinical development.