Associate Medical Data Review Manager

Company Overview

We all have know about IQVIA not because its works in clinical research and research and development field but the reality is IQVIA is a leading global healthcare and life sciences company that is helping the pharmaceutical sector in  making smarter decisions through data, technology, advanced analytics, and clinical research expertise.

IQVIA works closely with healthcare organizations, Pharmaceutical companies, medical devices and biotechnology firms to improve patient health and helps in bringing better treatments to the market

IQVIA has its strong presence across healthcare and life sciences domain from clinical development and real-world evidence to commercial strategy, regulatory support, safety solutions, and healthcare technology, IQVIA supports organizations during every phase of the product lifecycle.

IQVIA offers an positive environment for professionals where medical knowledge, scientific thinking, data interpretation, and operational excellence come together. Candidates joining IQVIA get the opportunity to contribute to real time healthcare projects, work with global teams, and build exposure to international standards in clinical research and data management.

IQVIA also focuses strongly on innovation, using AI related to healthcare, analytics platforms, and digital solutions to improve the way of data collection in clinical and healthcare setting, reviewed, and used. This makes IQVIA an amazing workplace for candidates who want to grow in clinical research, medical review, data sciences, pharmacovigilance, regulatory affairs, medical affairs, or healthcare consulting.

Job Summary

The Medical Reviewer role is to ensure that the patient data collected during clinical trials is medically correct, and complete. You will review patient data from a clinician point of view. If any gap, unusual findings, inconsistencies, safety concerns that may require clarification. Support in data management and ensure that clinical data meets the expectations of stakeholder.

You will be responsible for medical history review, laboratory data, diagnosis, adverse events, drugs and other clinical information.

Work closely with clinical data management teams, medical monitors, pharmacovigilance teams and project stakeholders to support query generation, query resolution, documentation and timely completion of review activities.

This position is a great opportunity for candidates want to utilize their medical or clinical knowledge in the clinical research industry. It provides an opportunity to understand the process of reviewing patient data, cleaned, and validated during clinical trials.

Key Responsibilities

Review of Patient Data
Review of clinical data to identify anomalies, irrelevant medical findings, and gaps in patient information. Ensure data is clinically logical, protocol-compliant, and medically plausible.

Protocol-Based Data Evaluation
Assessing patient data according to the need of study protocol, therapeutic area, and clinical expectations. Identify discrepancies that may require clarification from the site or clinical study team.

Project Management Support
Provide support to clinical study teams in management related work like query resolution, workload planning and process improvement. 

Cross-Functional Collaboration
Coordination with Clinical Data Management, Pharmacovigilance, Medical Monitoring, Clinical Operations and other departments. Timely communication and resolution of medical review or data concerns.

Customer and Compliance Support
Support in projects according to the requirement to maintain strong customer relationships. Timely follow-up and resolution of issues and escalation to ensure study quality and regulatory compliance.

Service Performance and Quality Improvement
Track service quality, performance metrics, and timelines under guidance. Support root-cause analysis, corrective actions, and continuous improvement of task efficiency and deliverable quality.

Subject Matter Expertise
Subject Matter Expert by providing medical, clinical, and therapeutic area guidance to project teams for better reach. Support decision-making through strong clinical knowledge and structured data review insights.

Training and Meeting Participation
You will be responsible for Providing training to clinical project teams related to therapeutic area or indication-specific field if required. Involvement in kick-off meetings, weekly team meetings, and client meetings to discuss study progress, findings, issues, and deliverables.

Qualifications and Skills

Must-Have Skills

• MBBS with at least 2+ years of relevant experience, or MD with any experience/fresher

• Strong understanding of medical and clinical data

• Strong knowledge of medical terminology, anatomy and physiology, and pharmacology

• Experience in clinical data in a CRO, pharmaceutical company or other medical field

• Ability to interpret medical data accurately and awareness of metrics, status updates and performance indicators to allow timely decision making

• Ability to identify issues, take appropriate action, and support resolution of medical or data-realted concerns

• Ability to work with minimal supervision by using available resources effectively

Bonus Skills

• Must have leadership experience in a CRO, Pharmaceutical or any medical setting

• Strong project management skills to support timelines, team coordination

• Skills to guide, support, and train other teams if required

• Ability to work on multiple projects effectively

• Experience of working with clinical study teams, internal stakeholders, managers and clients

• Contribution in process improvement and quality enhancement activities

Soft Skills & Personality Traits

• Excellent Communication skills

• Customer-focused mindset

• Collaborative Teamwork

• Problem-solving

• Relationship-building

• Proactive approach

• Detail-oriented

• Adaptable

Salary and Benefits

IQVIA offers a salary range of ₹10 LPA to ₹15 LPA for this role and it may vary depending on your previous experience, domain knowledge, skills and it also provides other benefits like insurance coverage, monthly health, and annual health check-ups, and structured career development opportunities.

Location

This is full time hybrid role based in Bengaluru, India, with an additional location in Thane, Mumbai.

Career Growth Opportunities

This role offers a growth as well as strong foundation in the clinical domain.

You may get a lot of experience related to clinical data review, medical monitoring, project management, and therapeutic area.

Team Structure

You will work closely with clinical study teams, pharmacovigilance team and other departments to ensure smooth workflow.

Why This Role Stands Out

Medical reviewer role is ideal for those excited about clinical data, patient cases, and medical decision-making beyond hospital setting and have strong interest in clinical data review, and patient care.

How to Apply

IQVIA is looking for candidates who are excited to apply medical review expertise to clinical trials, structured patient data review, and high-quality data management from a clinician’s perspective.
Add keywords to your CV such as:

• Clinical documentation

• Therapeutic area expertise

• Lab value interpretation

• Adverse event evaluation

• Protocol adherence

• Anomaly detection

• Patient data analysis

Keep your CV clear and well-structured and then hit the apply button.

All the best!!!