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Clinical Data Review Associate (Mumbai)

Medpace
Medpace
0-2 years
Not Disclosed
10 Nov. 18, 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

Job Title: Clinical Data Review Associate

Location: Navi Mumbai, India (Office-Based)

Department: Data Management

Experience Required: Entry-level to 2+ years in clinical data review or clinical research

About the Role:
Medpace, a leading global full-service clinical Contract Research Organization (CRO), is seeking a Clinical Data Review Associate to join our Data Management team in Navi Mumbai. This role is ideal for nursing professionals or life sciences graduates who want to develop a career in clinical data management while contributing to high-quality clinical trials across multiple therapeutic areas.

As a Clinical Data Review Associate, you will play a key role in ensuring data integrity, reviewing clinical trial data, generating queries, and supporting the project team in maintaining compliance and accuracy.

Key Responsibilities:

  • Review clinical data collected from ongoing trials to ensure accuracy and completeness.

  • Generate and resolve queries to address inconsistent or missing clinical data.

  • Assist in developing clinical review guidelines to standardize processes.

  • Collaborate with project teams to communicate findings, trends, and recommendations.

  • Maintain adherence to internal SOPs and regulatory requirements throughout data review.

Qualifications & Skills:

  • Nursing degree (B.Sc Nursing or equivalent) or relevant life sciences qualification.

  • Basic understanding of clinical trial processes; familiarity with clinical data management is a plus.

  • Strong attention to detail and analytical thinking.

  • Effective communication and team collaboration skills.

  • Ability to manage multiple tasks in a fast-paced environment.

  • Both entry-level and experienced candidates are encouraged to apply.

Why Join Medpace:

  • Work in a flexible, office-based environment with opportunities for professional growth.

  • Competitive compensation, benefits, and paid time off (PTO) packages.

  • Structured career paths with access to training and mentorship.

  • Engage in meaningful work that impacts patient safety and therapeutic development globally.

  • Participate in employee health, wellness, and appreciation initiatives.

About Medpace:
Medpace is a global CRO providing Phase I-IV clinical development services to biotechnology, pharmaceutical, and medical device companies. With expertise across oncology, cardiology, metabolic disease, endocrinology, CNS, anti-viral, and anti-infective therapies, Medpace leverages scientific rigor and local regulatory knowledge to accelerate the development of safe and effective therapeutics. Headquartered in Cincinnati, Ohio, Medpace employs over 5,000 professionals across 40+ countries.

Awards & Recognition:

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

  • CRO Leadership Awards by Life Science Leader magazine

How to Apply:
Qualified candidates will be contacted for next steps following a review of their application. Submit your resume to Medpace’s HR team to join a global organization advancing clinical research.

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