PHARMAFull-time
Medical Data Reviewer
BANGALORE (IN)REMOTEPOSTED: 9/23/2026
PHARMAFull-time
HIRING ORGANIZATIONICONContract Research Organization (CRO) / Clinical Research / Healthcare Services
ROLE OVERVIEW
Provide expert medical oversight of clinical trial data, ensuring accuracy, consistency, and patient safety in a sponsor-dedicated model.
ROLE DEFINITION & RESPONSIBILITIES
- •Conduct medical review of clinical trial data as per Medical Data Review Plan using listings and patient profiles
- •Collaborate with Medical Lead and Clinical Research Scientist to coordinate medical data review and manage queries
- •Review data for protocol deviations, raising queries to sites, and following them until resolution
- •Provide input into eCRF, CRF Completion Guidelines, edit checks, and review plans
- •Collaborate with relevant functions to improve quality of clinical data review, subject safety, and data integrity
Reporting Hierarchy: Reports to Medical Lead / Clinical Research Scientist • Sponsor-dedicated project team
QUALIFICATIONS & REQUIREMENTS
REQUIRED QUALIFICATIONS
- Degree in a medical profession or life sciences (physician, nurse, pharmacist, scientist)
- >2 years of experience in pharmaceutical industry, CRO, or healthcare as a Medical Data Reviewer or similar role
- Fundamental knowledge of GCP/ICH guidelines, clinical trial design, and statistics
- Proficient English in written/verbal communication
PREFERRED QUALIFICATIONS
- •PhD, MBBS, BDS, MD strongly preferable
- •Educational and/or work experience in oncology, neurology, and/or immunology
- •Experience in analysis and interpretation of clinical data and working knowledge of biostatistics
REQUIRED VERIFIED SKILLS
Medical Data Review
Clinical Research
Good Clinical Practice (GCP)
ICH Guidelines
Data Integrity
Oncology
Neurology
Immunology
COMPENSATION & REWARDS
Salary: Competitive / Disclosed upon candidate shortlisting
Benefits: Competitive base salary, health and wellbeing programs, retirement plans, learning and development opportunities
Competitive compensation package benchmarked against top clinical research organizations in India.
ORGANIZATION CONTEXT & CULTURE
ICON is the world’s largest FSP clinical research organisation supporting pharmaceutical and medical device partnerships globally.
TEAM SIZE: 10,000+ employees
INDUSTRY: Contract Research Organization (CRO) / Clinical Research / Healthcare Services
Culture: ICON fosters a collaborative and supportive global work environment focused on career development and patient wellbeing.
EXPECTED CAREER ROADMAP
Clear pathways for career development within global clinical operations and FSP sponsor-dedicated pathways at ICON.
APPLICATION ADVISORY
Highlight your specific therapeutic experience (e.g., oncology or neurology) and familiarity with clinical data review plans and patient profiles.
RECOMMENDED TRAINING
1/5
READY TO SUBMIT?
Verify your capability profile and matching credentials before submitting direct applications.