Associate Medical Data Review Manager Job at IQVIA. MBBS and MD candidates can explore clinical data careers in India
Are you a medical professional looking to move into clinical research, medical data review, or pharmacovigilance-related roles? This is an excellent opportunity to work with a global healthcare leader in a role that blends clinical expertise with data analysis and project management. IQVIA is currently hiring Associate Medical Data Review Managers in India, offering exposure to clinical trials, patient data evaluation, and cross-functional collaboration.
Company Overview
IQVIA is a global leader in healthcare analytics, clinical research services, and commercial insights for the life sciences industry. The organization partners with pharmaceutical, biotechnology, and healthcare companies to accelerate drug development and improve patient outcomes. With a strong emphasis on data-driven decision-making, IQVIA provides innovative solutions across clinical trials, real-world evidence, and healthcare intelligence.
Job Overview
| Job Title | Associate Medical Data Review Manager |
|---|---|
| Company | IQVIA |
| Location | Bangalore & Thane, India |
| Employment Type | Full-Time |
| Department | Medical Data Review / Clinical Data Sciences |
| Experience | MBBS with 2+ years / MD Freshers Eligible |
| Qualification | MBBS / MD |
| Application Deadline | March 25, 2026 |
| Job Requisition ID | R1458281 |
Job Location & Employment Type
- Work Locations: Bangalore (Karnataka) and Thane (Maharashtra)
- Job Type: Full-time
- Work Setup: Office-based with collaboration across global teams
Open Positions / Department Details
The role is part of the Medical Data Review / Clinical Data Sciences function. Professionals in this team ensure the accuracy, consistency, and medical validity of patient data collected during clinical trials.
Key Roles & Responsibilities
As an Associate Medical Data Review Manager, you will play a critical role in maintaining the quality and integrity of clinical trial data. Your responsibilities will include:
Medical Data Review & Analysis
- Reviewing patient-level clinical data to ensure medical consistency and plausibility
- Identifying anomalies or discrepancies in patient records as per study protocols
- Applying clinical knowledge to validate data accuracy
Project Management & Coordination
- Supporting project management activities across clinical study teams
- Collaborating with internal teams, stakeholders, and decision-makers
- Monitoring workflows, timelines, and workload projections
- Escalating issues and ensuring timely resolution
Quality & Compliance
- Tracking service performance and identifying root causes of data issues
- Implementing corrective and preventive actions
- Ensuring compliance with clinical protocols and regulatory standards
- Following up on compliance-related concerns until closure
Subject Matter Expertise
- Acting as a Subject Matter Expert (SME) for medical data review processes
- Providing therapeutic area training to clinical and data teams
- Offering clinical insights to improve study outcomes
Process Improvement & Team Support
- Identifying opportunities to enhance efficiency and quality of deliverables
- Participating in project meetings, including kick-offs and client discussions
- Supporting cross-functional teams with clinical expertise
- Maintaining strong professional relationships with clients and internal teams
Eligibility Criteria
Educational Qualification
Candidates must have one of the following:
- MBBS (Bachelor of Medicine, Bachelor of Surgery)
- MD (Doctor of Medicine)
Experience Required
- MBBS candidates: Minimum 2 years of relevant experience
- MD candidates: Freshers or experienced candidates can apply
- Experience in:
- Clinical data sciences
- CRO or pharmaceutical industry
- Medical or clinical environments
Skills Required
- Strong understanding of:
- Medical terminology
- Pharmacology
- Human anatomy and physiology
- Knowledge of clinical trial processes and data review
- Excellent analytical and problem-solving skills
- Strong project management and organizational abilities
- Effective communication and interpersonal skills
- Ability to manage multiple projects simultaneously
- Customer-focused mindset and teamwork skills
- Ability to work independently with minimal supervision
Salary & Benefits
- Salary will be as per company norms
- Additional benefits may include:
- Health insurance coverage
- Career growth in clinical research and data sciences
- Exposure to global clinical trials
- Learning and development opportunities
Selection Process
The hiring process may include:
- Resume screening
- HR interview
- Technical/medical interview
- Final discussion with senior management
How to Apply
Interested and eligible candidates should apply through the official IQVIA careers portal.
- Ensure all details provided in the application are accurate and complete
- Update your resume with relevant clinical or research experience

Important Dates
- Last Date to Apply: March 25, 2026
- Apply early to avoid missing the deadline
Why Apply for This Pharma Job?
This role is ideal for medical professionals who want to transition beyond clinical practice into the pharmaceutical and clinical research industry. Benefits include:
- Opportunity to work on global clinical trials and patient data
- Development of expertise in clinical data review and validation
- Exposure to international regulatory standards and processes
- Career growth in high-demand domains like CROs and pharma companies
- Collaborative work environment with experienced professionals
Important Note / Disclaimer
IndiaPharmaJobs.in is an independent job information platform. We are not affiliated with IQVIA or any employer mentioned above. We do not charge any fees for job applications. Candidates are advised to verify job details from the official website before applying.
Final Call-to-Action
If you are an MBBS or MD professional looking to build a rewarding career in clinical research and data sciences, this is your opportunity. Apply now and take the next step in your pharma career with a global organization.