Location: Bangalore, India
Company: IQVIA
Job Type: Full-Time
Application Deadline: June 30, 2026
Job Requisition ID: R1535675
Experience Required: 3–6 years (Freshers are not eligible)
About the Company
IQVIA is a leading global provider of clinical research services, healthcare analytics, and commercial insights. The organization plays a pivotal role in accelerating drug development and improving patient outcomes through data-driven intelligence and innovative clinical solutions.
Job Overview
The Associate Medical Data Review Manager is responsible for delivering high-quality medical data review and clinical data management support across clinical trials. This role combines medical expertise with project management capabilities to ensure data accuracy, protocol compliance, and operational efficiency from a clinical perspective.
Key Responsibilities
Perform structured medical review of patient data to ensure clinical accuracy, consistency, and protocol compliance
Identify patient-level anomalies and ensure medical plausibility within clinical datasets
Collaborate with cross-functional clinical study teams, stakeholders, and internal departments to drive project execution
Manage workflow processes including issue escalation, workload planning, and continuous improvement initiatives
Maintain strong client relationships and ensure high levels of customer satisfaction
Monitor service performance metrics and contribute to root cause analysis and corrective actions
Ensure timely identification, tracking, and resolution of compliance-related issues
Act as a Subject Matter Expert (SME) for medical data review processes
Deliver therapeutic area and indication-based training to clinical teams
Participate in study kick-off meetings, client discussions, and regular project review meetings
Required Qualifications
MBBS or equivalent medical degree is mandatory
Alternatively, a Bachelor’s degree in Life Sciences with a minimum of 3 years of relevant clinical research or clinical practice experience
Total experience requirement: 3–6 years in clinical data science, medical review, or related domain
Prior experience in a CRO, pharmaceutical company, or healthcare organization preferred
Strong understanding of clinical/medical data and data review processes
Sound knowledge of medical terminology, pharmacology, anatomy, and physiology
Ability to interpret clinical data with both scientific and operational perspectives
Excellent communication, stakeholder management, and teamwork skills
Strong analytical, problem-solving, and project management capabilities
Ability to manage multiple projects and work independently with minimal supervision
Key Skills and Competencies
Clinical Data Review and Medical Monitoring
Clinical Data Management and Data Integrity
Project Management and Process Optimization
Regulatory Compliance and Quality Assurance
Stakeholder Communication and Client Management
Why This Role Matters
This role is critical in ensuring the accuracy, reliability, and scientific integrity of clinical trial data. As part of a globally recognized organization, you will contribute directly to the development of innovative therapies and improved healthcare outcomes.
Important Note for Applicants
This is a mid-level role requiring prior experience in clinical research or medical data review. Freshers are advised to apply for entry-level roles such as Clinical Data Associate, Pharmacovigilance Associate, or Clinical Research Coordinator before progressing to this position.
How to Apply
Apply directly through the official careers portal of IQVIA or explore verified global opportunities on ThePharmaDaily.com.
Fraud Prevention Disclaimer
IQVIA follows a strict zero-tolerance policy against recruitment fraud. Candidates must ensure all submitted information is accurate and verifiable. Any misrepresentation may lead to disqualification or termination as per applicable regulations.
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