Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Clinical Nurse Reviewer I

Icon Plc
ICON PLC
2-5 years
preferred by company
Chennai, India
1 May 18, 2026
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/Life Sciences Skills: CPC Certified, Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines

Clinical Nurse Reviewer I

Location: Chennai, India
Company: ICON plc
Job Type: Full-Time
Work Mode: Office With Flex (Hybrid)
Department: Clinical Research / Clinical Operations / Endpoint Adjudication
Job Reference ID: JR145827
Industry: Clinical Research | CRO | Pharmaceutical | Biotechnology | Medical Device

Job Overview

ICON plc is hiring a Clinical Nurse Reviewer I for its clinical research operations team in Chennai. This opportunity is ideal for qualified nursing professionals with experience in clinical research, endpoint adjudication, clinical data review, patient safety documentation, medical record analysis, and regulatory clinical trial compliance.

As a Clinical Nurse Reviewer, you will support endpoint-driven clinical trials by reviewing clinical source documentation, preparing adjudication packages, analyzing medical data, and coordinating with project management and clinical operations teams. This role is critical in ensuring high-quality endpoint adjudication, accurate case review, and regulatory-compliant clinical trial execution.

This opportunity is ideal for professionals seeking career growth in clinical research nursing, endpoint adjudication, clinical data review, pharmacovigilance-adjacent roles, and global CRO operations.

Key Responsibilities

Clinical Endpoint Documentation Review

  • Review clinical trial endpoint source documentation for completeness, medical accuracy, and adjudication readiness.
  • Ensure high-quality clinical content review for physician adjudication committees.
  • Support objective endpoint assessment in endpoint-driven trials.

Adjudication Package Management

  • Collect, organize, quality check, and maintain adjudication packages.
  • Ensure dossiers contain medically complete and logically structured documentation.
  • Coordinate timely collection of all required endpoint documentation.

Medical Case Review & Analysis

  • Interpret:
    • Medical conditions
    • Clinical procedures
    • Laboratory data
    • Adverse event information
    • Source clinical documentation

Support accurate clinical endpoint determination.

Clinical Narrative Writing

  • Prepare clear, medically accurate clinical narrative summaries.
  • Document endpoint case details for adjudication review.
  • Ensure structured and consistent clinical reporting.

Clinical Data Coding & Database Management

  • Support coding activities using:
    • MedDRA terminology

Maintain endpoint committee database records accurately and consistently.

Query Resolution & Stakeholder Coordination

  • Respond to clinical queries from:
    • Physician adjudicators
    • Clinical site personnel
    • Internal project teams
    • Clinical operations stakeholders

Ensure timely issue resolution and documentation follow-up.

Clinical Reporting & Progress Tracking
Support generation of:

  • Case status reports
  • Progress tracking reports
  • Committee performance reports
  • Quality metrics
  • Periodic operational updates

Regulatory Compliance
Ensure adherence to:

  • Good Clinical Practice (GCP)
  • Federal clinical research regulations
  • International clinical trial standards
  • Company SOPs
  • Endpoint adjudication quality requirements

Risk & Quality Oversight

  • Identify potential sources of unblinding.
  • Support quality review of adjudication workflows.
  • Ensure data integrity and inspection readiness.

Required Educational Qualification
Mandatory:

  • Registered Nurse (RN)

Preferred additional backgrounds:

  • Clinical nursing
  • Healthcare sciences
  • Clinical research nursing

Experience Required

  • Minimum 2+ years of relevant experience
  • Freshers are not eligible

Relevant experience includes:

  • Clinical research
  • Drug development
  • Clinical trial operations
  • Endpoint adjudication
  • Medical review
  • Clinical documentation review

Preferred experience:

  • Clinical data management
  • Pharmacovigilance-related documentation review
  • Endpoint committee operations

Required Skills

  • Clinical Research
  • Clinical Documentation Review
  • Endpoint Adjudication
  • Medical Record Review
  • Clinical Data Analysis
  • Clinical Narrative Writing
  • MedDRA Coding
  • Patient Safety Documentation
  • Query Management
  • GCP Compliance
  • Regulatory Documentation
  • Clinical Reporting
  • Medical Interpretation
  • Data Quality Review