Clinical Data Review Associate – Data Management (Nursing Background Preferred)
Location: Navi Mumbai, India
Department: Clinical Data Management
Job ID: 12326
Employment Type: Full-Time (Office-Based)
Company: Medpace (Global CRO)
ThePharmaDaily.com is featuring an excellent opportunity for Clinical Data Review Associates in Mumbai. This role is ideal for entry-level and experienced nurses seeking to transition into Clinical Data Management within a global Contract Research Organization (CRO) environment.
If you are looking to leverage your clinical knowledge in a structured clinical trial data review setting, this position offers a strong foundation for career growth in clinical research, pharmacovigilance, and regulatory data sciences.
Role Overview
The Clinical Data Review Associate will support the Data Management team by reviewing, validating, and querying clinical trial data to ensure accuracy, consistency, and regulatory compliance. The role involves collaboration with cross-functional clinical project teams and contributes directly to high-quality data delivery for Phase I–IV clinical studies.
Key Responsibilities
Clinical Data Review & Query Management
Review clinical data collected from investigational sites across global trials.
Identify inconsistencies, missing data, and protocol deviations.
Generate and resolve data queries in collaboration with investigative sites and project teams.
Ensure data integrity in accordance with ICH-GCP and regulatory standards.
Guideline Development & Process Support
Assist in development and refinement of clinical review guidelines.
Support continuous process improvement within data management workflows.
Analyze trends and escalate recurring data issues to relevant stakeholders.
Cross-Functional Collaboration
Interface with Clinical Operations, Biostatistics, Medical Review, and Project Management teams.
Communicate review findings and contribute to quality-driven decision-making.
Experience Required
Entry-level candidates with a Nursing degree are encouraged to apply.
Experienced nurses with prior exposure to:
Clinical trials
Clinical documentation review
Electronic Data Capture (EDC) systems
Clinical data validation
will have a competitive advantage.
0–3 years of experience in clinical research, hospital settings, or clinical data environments preferred.
Educational Qualification
Bachelor’s Degree or Diploma in Nursing (mandatory).
Registration with a recognized nursing council preferred.
Core Competencies & Skills
Foundational understanding of clinical trial processes.
Strong analytical and critical thinking skills.
Attention to detail and data accuracy.
Ability to interpret clinical notes and medical terminology.
Proficiency in English (written and verbal).
Ability to work effectively in a team-oriented environment.
Basic knowledge of clinical databases and electronic data capture systems preferred.
About the Organization
Medpace is a full-service global Clinical Research Organization (CRO) delivering Phase I–IV clinical development services to pharmaceutical, biotechnology, and medical device companies. With operations in 40+ countries and expertise across oncology, cardiology, metabolic diseases, CNS, infectious diseases, and endocrinology, Medpace supports accelerated development of safe and effective therapies worldwide.
Why Consider This Role
Structured career path within Clinical Data Management.
Opportunity to transition from clinical nursing to clinical research.
Exposure to global regulatory standards and multi-therapeutic clinical programs.
Competitive compensation and professional development opportunities.
This role is particularly suitable for nurses aspiring to build long-term careers in Clinical Data Management, Pharmacovigilance, Clinical Operations, or Regulatory Affairs within the pharmaceutical and CRO industry.
Explore more Clinical Research, Data Management, Pharmacovigilance, and Global CRO opportunities on ThePharmaDaily.com – your trusted global pharmaceutical career platform.
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