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Full Time

Associate Medical Data Review Manager

IQVIA
Bangalore
₹10 LPA - ₹15 LPA
Posted 02/06/2026

About the Role

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!!!

Market Insights & Trends

Salary Insights

The amount of money that gets paid can be different depending on how they have been working, where they live and what kind of job they are doing. Some places pay more than others. Most good jobs include extra money for doing a good job, health insurance and flexible hours. Companies pay high salary to make sure they can get the people they want.

Hiring Trends

The number of jobs for this profile is going up every year. Hospitals and other healthcare companies are looking for people who're good, at their job and can also figure out new problems. They want who can do the work and also think on their feet to deal with the challenges of working in healthcare today.

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Frequently Asked Questions

Everything you need to know about the process

Jobslly curates specialized corporate healthcare listings tailored for medical graduates seeking a career pivot. Instead of sifting through general medical job boards, doctors can use our platform to directly access high-paying non-clinical opportunities in Pharmacovigilance, Medical Writing, and Clinical Trial Management with top pharmaceutical companies and CROs. Most MBBS/BDS grads don't realise — clinical background is already enough to get into pharma. The problem is nobody explains this clearly. On Jobslly each listing shows salary range, fresher eligibility, and certifications worth getting before applying. Pharmacovigilance roles for example keep asking for RQAP-GCP. All this is on the listing itself, no separate research needed.
Yes. Jobslly features dedicated filtering for remote and hybrid healthcare roles, which are highly sought after by medical professionals looking for better work-life balance. Doctors can easily track and apply for verified work from home positions, such as Telehealth Consultants, Medical Chart Reviewers, and Drug Safety Associates, directly through the platform Real problem with remote medical jobs — half are fake, half are badly described. You join and realise it's a night shift for a US team nobody mentioned. Jobslly listings show shift timings, contract type, whether company gives equipment or WFH allowance. All upfront before you apply.
Generic job portals often bury specialized clinical roles under thousands of unrelated listings. Jobslly is purpose-built exclusively for the healthcare and health-tech sectors. We provide doctors with targeted career alerts for niche specialties, direct application routes to premium employers in major hubs like Mumbai and Bangalore, and real-time insights into medical salary benchmarks. Salary benchmark is something doctors switching careers genuinely need. No idea what number to quote, quote low, stuck with it forever. Jobslly shows pay ranges — by role, city, experience level. Career alerts are filtered by specialty and location so inbox isn't flooded with irrelevant stuff daily.
To protect medical professionals from recruitment fraud and unverified agencies, Jobslly operates a strictly vetted ecosystem. We exclusively partner with verified employers, prioritizing NABH-accredited hospitals, established health-tech innovators, and recognized multinational pharma brands so you can apply with complete confidence. Fake agencies, ghost listings, upfront fee scams — very common in medical recruitment, especially pharma and international roles. Jobslly doesn't allow unregistered agents on platform at all. Each listing shows actual audit date, not just an old generic verified badge. Suspicious listing — report button is there, compliance checks within 24 hours.
Yes. Backed by the Academically Global network, Jobslly goes beyond domestic job listings by providing access to structured International Placement Programs. We connect ambitious doctors, nurses, and clinical staff with credible, high-paying healthcare contracts in global markets like the UK, Australia, and the UAE, while outlining the necessary credentialing steps. UK needs PLAB, Australia needs AMC, UAE needs DHA or HAAD depending on emirate. Most doctors know this but the full picture — exam pattern, timeline, cost, official links — is scattered everywhere. Jobslly puts the credentialing roadmap directly on each international listing. Academically Global counsellors also available — people who've actually placed Indian doctors in these countries, know exactly where candidates get stuck.
Forget the assumption that only senior doctors make the big money. That's outdated. Right now, some of the best packages in Indian healthcare are going to people you wouldn't expect — Senior Medical Writers, Clinical Data Managers, Pharmacovigilance Specialists working with global pharma firms or CROs. These aren't rare unicorn jobs. They exist, they hire regularly, and the salaries are negotiable in ways hospital jobs rarely are. Most candidates just don't know to look for them.
Not all cities are equal on this front, and applying blindly wastes time. Bangalore is where health-tech and clinical research hiring is concentrated. Hyderabad is pharma country – manufacturing, QC, formulation, R&D. Mumbai and Navi Mumbai handle specialized hospital care, advanced nursing roles, and pharmacovigilance admin, medical writing, policy work all coexist there without one dominating the other. If you're open to relocating, knowing this upfront changes which jobs you even bother applying for.
Both. That's the honest answer. Legitimate remote roles in healthcare have existed long before anyone started calling things "hybrid." Medical Coders, Pharmacovigilance Associates, Telehealth Coordinators, Freelance Medical Writers — these positions have been hiring remotely for years through companies that are very much real. The fake ones almost always have one thing in common: they ask for money. Registration fees, document processing charges, security deposits — whatever the label, it's a scam. No actual employer takes money from a candidate before they join. That rule holds without exception.
EMR platforms, digital documentation tools, data tracking systems, AI-assisted reporting software. These aren’t “nice to have” anymore. They’re baseline. Clinical Knowledge is still the foundation but walking into an interview unable to navigate the systems the team uses daily is a problem. Candidates who are already familiar with these tools don’t need to be trained from scratch, and that matters when hiring managers are comparing two otherwise similar profiles.
Short answer: yes, and it's happening constantly. Long answer: it depends on what you want. If structured hours, no emergency calls, and a salary that doesn't plateau after three years sound appealing — corporate healthcare is worth your attention. Medical Writing, Drug Safety Review, Insurance Auditing, Health-tech Program Management — these roles specifically want people who understand clinical realities. A nursing degree or MBBS isn't a handicap here. It's often the reason you get the interview.