Location: Bangalore, India
Company: IQVIA
Job ID: R1535680
Employment Type: Full-Time
Application Deadline: April 28, 2026
Experience Required: 3–6 Years (Not suitable for freshers)
About the Company
IQVIA is a global leader in clinical research services, healthcare analytics, and commercial insights for the life sciences industry. The organization leverages advanced data science and domain expertise to accelerate drug development, improve patient outcomes, and drive innovation across global healthcare systems.
Job Overview
The Associate Medical Data Review Manager is responsible for ensuring the accuracy, consistency, and clinical relevance of patient-level data in clinical trials. This role combines medical expertise with project management skills to support structured patient data review, ensuring protocol compliance and high-quality data delivery.
Key Responsibilities
Perform structured medical data review to ensure clinical consistency and protocol adherence
Identify patient-level anomalies and ensure medical plausibility of clinical trial data
Collaborate with clinical study teams, stakeholders, and internal departments to manage workflows and improve processes
Support project management activities including workload forecasting, issue escalation, and performance tracking
Maintain strong client relationships and ensure high-quality service delivery
Track key performance metrics and identify root causes of operational issues, implementing corrective actions
Ensure timely resolution of compliance and data quality issues
Act as a Subject Matter Expert (SME) for medical data review processes
Provide therapeutic area and indication-specific training to clinical teams
Participate in project kick-off meetings, team discussions, and client interactions
Required Qualifications
MBBS or equivalent medical degree preferred
OR Bachelor’s degree in Life Sciences, Clinical Research, or related field with relevant experience
3–6 years of experience in clinical practice, clinical research, or medical data review
Strong understanding of clinical data, medical terminology, pharmacology, anatomy, and physiology
Prior experience in CRO, pharmaceutical, or healthcare environment is highly preferred
Demonstrated ability in project management and leadership support
Excellent communication, interpersonal, and stakeholder management skills
Strong analytical thinking and problem-solving abilities
Ability to manage multiple projects and work independently with minimal supervision
Key Skills and Competencies
Clinical Data Review and Medical Monitoring
Patient Data Analysis and Risk Identification
Project Management and Process Improvement
Clinical Trial Operations and Compliance
ICH-GCP and Regulatory Understanding
Cross-functional Collaboration and Client Management
Why This Role Stands Out
Opportunity to work with one of the world’s leading clinical research organizations
Exposure to global clinical trials and advanced data-driven healthcare solutions
Strong career growth in medical data review, clinical research, and pharmacovigilance domains
Collaborative environment with cross-functional global teams
Important Note for Applicants
This is a mid-level role requiring prior experience in clinical research or medical data review. Freshers are advised to begin with entry-level roles such as Clinical Data Associate, Pharmacovigilance Associate, or Clinical Research Coordinator before progressing to managerial positions.
How to Apply
Interested candidates can apply through the official careers page of IQVIA or explore more verified global opportunities on ThePharmaDaily.com.
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