ICON is inviting applications for the position of Medical Data Reviewer in Bangalore, India, with a remote/home-based work option. This opportunity is ideal for experienced professionals in clinical research, pharmacovigilance, medical monitoring, clinical data review, and drug development who want to contribute to global clinical trials across oncology, neurology, immunology, and other therapeutic areas.
If you have experience reviewing clinical trial data, ensuring patient safety, interpreting medical information, and collaborating with multidisciplinary clinical teams, this ICON Medical Data Reviewer Job 2026 offers an excellent opportunity to advance your career in one of the world’s leading CROs.
Job Overview
| Particular | Details |
|---|---|
| Company | ICON plc |
| Job Title | Medical Data Reviewer |
| Job ID | JR156093 |
| Location | Bangalore, India |
| Work Mode | Remote / Home-Based |
| Job Type | Full-Time |
| Experience | 2+ Years |
| Department | Clinical Research |
| Therapeutic Areas | Oncology, Neurology, Immunology & Others |
About ICON
ICON is a leading global healthcare intelligence and clinical research organization dedicated to accelerating the development of innovative medicines and therapies. The company partners with pharmaceutical, biotechnology, and medical device organizations worldwide to improve patient outcomes through high-quality clinical research.
Key Responsibilities
As a Medical Data Reviewer at ICON, you will:
- Perform medical review of Phase IโIII clinical trial data.
- Review patient profiles and clinical data listings for completeness and medical plausibility.
- Identify inconsistencies, missing data, and protocol deviations.
- Raise and manage medical queries with investigative sites.
- Support interim analyses, database lock activities, and post-lock reviews.
- Collaborate with Medical Leads and Clinical Research Scientists.
- Review clinical safety and efficacy data using established medical review plans.
- Interpret oncology, neurology, immunology, and other therapeutic clinical data.
- Contribute to Medical Data Review Plans, edit checks, and CRF Completion Guidelines.
- Assist with patient narratives and Trial Master File (eTMF) documentation when required.
- Ensure compliance with ICH-GCP, regulatory guidelines, and study protocols.
- Identify clinical trends and recommend data quality improvements.
Eligibility Criteria
Candidates should have:
- More than 2 years of experience in Clinical Research Organizations (CROs), pharmaceutical companies, healthcare, Medical Monitoring, or Medical Data Review.
- Experience reviewing global clinical trial data.
- Knowledge of clinical trial design and drug development.
- Understanding of medical review methodologies.
- Experience interpreting clinical safety and efficacy data.
- Strong analytical and problem-solving skills.
- Excellent written and verbal English communication.
- Experience with clinical databases and electronic Case Report Forms (eCRFs).
- Knowledge of patient profiles, medical listings, RECIST 1.1, CTCAE grading, and related clinical criteria.
- Familiarity with biostatistics, regulatory requirements, and GCP.
Educational Qualification
Eligible candidates include professionals with:
MBBS, MD, BDS, PhD, B.Pharm, M.Pharm, Pharm.D, B.Sc Nursing, M.Sc Nursing, MSc Life Sciences, PhD Life Sciences, or other medical/life sciences degrees.
Preferred Qualifications
- MBBS
- MD
- BDS
- PhD
- Medical professionals with oncology, neurology, or immunology experience
Preferred Skills
- Medical Data Review
- Clinical Research
- Clinical Data Management
- Medical Monitoring
- Clinical Trial Operations
- Oncology
- Neurology
- Immunology
- ICH-GCP
- Clinical Safety
- Biostatistics
- Protocol Deviation Review
- Patient Profiles
- eCRF Review
- Medical Queries
- Data Integrity
- Clinical Database Review
Salary (Estimated)
Based on similar Medical Data Reviewer positions in India, the estimated salary is:
โน12 LPA โ โน22 LPA
Actual compensation depends on qualifications, therapeutic expertise, and experience.
Employee Benefits
ICON offers:
- Competitive salary
- Annual performance incentives
- Medical insurance
- Dental & vision benefits (where applicable)
- Retirement and pension plans
- Life insurance
- Disability coverage
- Employee Assistance Program (EAP)
- Learning & development programs
- Structured career progression
- Flexible remote working opportunities
Why Join ICON?
- Work remotely on global clinical trials.
- Collaborate with international clinical research teams.
- Gain exposure to oncology, neurology, and immunology studies.
- Enhance expertise in medical data review and clinical development.
- Excellent learning and career advancement opportunities.
How to Apply

