ICON plc Hiring: Medical Data Reviewer (Oncology / Neurology / Immunology)

ICON plc is inviting applications for the position of Medical Data Reviewer based in Bengaluru, Karnataka.

This subject matter expert role is responsible for ensuring the medical integrity, safety, and plausibility of Phase I–III clinical trial data across therapeutic areas such as oncology, neurology, and immunology in full compliance with GCP/ICH guidelines and global regulatory standards.

Key Job Details

Designation: Medical Data Reviewer
Company: ICON plc
Experience Required: 2+ years of relevant experience
Location: Bengaluru, Karnataka
Education: Degree in Medicine or Life Sciences (MBBS, MD, BDS, PhD, or Pharmacy / Nursing / Clinical Sciences)
Functional Area: Medical Data Review / Clinical Operations
Industry Sector: Clinical Research / Healthcare / Pharma
Application Deadline: 30 October 2026

Core Responsibilities

Clinical Data Review & Query Management: Conduct medical evaluation of patient profiles, incremental listings, and data visualization tools according to the Medical Data Review Plan; identify data inconsistencies, protocol deviations, and missing clinical events, raising and resolving site queries.
Milestone & Database Lock Support: Partner closely with Medical Leads and Clinical Research Scientists to ensure clinical data is medically sound ahead of critical milestones, such as interim analyses, Data Monitoring Committee (DMC) reviews, health authority submissions, and final database locks.
Specialized Safety & Efficacy Assessment: Interpret cancer diagnoses, RECIST 1.1 response criteria, CTCAE adverse event gradings, concomitant medications, and clinical safety endpoints.
Documentation & Strategy: Provide clinical inputs into eCRF design, CRF Completion Guidelines, edit check specifications, and Medical Data Review Plans; assist with patient safety narratives and maintain trial documentation in the electronic Trial Master File (eTMF).

Candidate Profile & Qualifications

Education: Degree in a medical profession or life sciences (MBBS, MD, BDS, PhD, or Master’s/Bachelor’s in Pharmacy/Nursing/Life Sciences).
Experience: Minimum 2 years within a CRO, pharma company, or clinical setting as a Medical Data Reviewer, Medical Monitor, or related scientific role.
Therapeutic Expertise: Working knowledge in clinical oncology, neurology, or immunology trial designs is strongly preferred.
Technical Skills: Familiarity with clinical databases, biostatistical analysis methodology, trend identification, and regulatory requirements (ICH-GCP).
Communication Skills: Excellent written and oral English communication for cross-functional meetings and medical query resolution.