Location: Chennai, India (Office with Flex / Hybrid)
Company: ICON plc
Job ID: JR145827
Job Type: Full-Time
Experience Required: Fresher or Minimum 2+ years (suitable for freshers)
About the Company
ICON plc is a globally recognized healthcare intelligence and clinical research organization supporting pharmaceutical, biotechnology, and medical device companies across the entire drug development lifecycle. With a strong focus on innovation, patient-centricity, and operational excellence, ICON plays a critical role in accelerating clinical development and improving patient outcomes worldwide.
Job Overview
The Clinical Nurse Reviewer I is responsible for supporting clinical trial endpoint adjudication processes by reviewing, compiling, and validating clinical data and source documentation. This role involves close collaboration with Project Management teams, Clinical Endpoint Committees, and cross-functional stakeholders to ensure accurate and high-quality clinical trial outcomes.
This position is ideal for experienced registered nurses with a background in clinical research, drug development, or medical data review who are looking to advance their careers in the global CRO industry.
Key Responsibilities
Ensure timely collection, review, and quality control of clinical endpoint documentation for adjudication
Compile medically accurate and complete adjudication dossiers for Clinical Endpoint Committees
Perform clinical content review of source documents to support endpoint validation
Respond to queries from physician adjudicators, clinical sites, and internal teams
Generate and track status reports, performance metrics, and quality indicators for adjudication activities
Collaborate with Clinical Operations and Project Management teams to ensure seamless trial execution
Identify potential risks such as unblinding and ensure compliance with study protocols
Interpret medical data including lab results, procedures, and patient conditions
Prepare narrative summaries and ensure accurate coding using MedDRA terminology
Maintain strict adherence to ICH-GCP guidelines, regulatory requirements, and company SOPs
Required Qualifications and Skills
Registered Nurse (RN) qualification is mandatory
Minimum 2+ years of experience in clinical research, drug development, or clinical data review
Strong understanding of clinical trials, endpoint adjudication, and regulatory standards
Experience with MedDRA coding and FDA regulatory requirements preferred
Familiarity with electronic data capture systems (eCRFs) and clinical databases
Proficiency in Microsoft Office tools and clinical documentation systems
Excellent analytical, critical thinking, and organizational skills
Strong written and verbal communication abilities
Willingness to travel up to 10% if required
Why Consider This Opportunity
Work with a globally established CRO on high-impact clinical trials
Gain exposure to endpoint adjudication and advanced clinical data review processes
Collaborative and growth-oriented work environment
Continuous learning and professional development opportunities
Competitive compensation and comprehensive employee benefits
Benefits and Work Culture
ICON offers a structured and employee-focused work environment with a strong emphasis on career development, work-life balance, and wellbeing. Employees benefit from competitive compensation packages, health insurance, retirement planning, global assistance programs, and flexible benefits tailored to individual needs.
The organization promotes diversity, inclusion, and equal opportunity, ensuring a workplace free from discrimination and supportive of all professionals.
Important Note for Applicants
This role requires prior clinical research or healthcare experience and is not open to freshers. Candidates with nursing backgrounds and exposure to clinical trials, pharmacovigilance, or medical data review will be highly preferred.
How to Apply
Interested candidates can apply through the official careers portal of ICON plc or explore more verified global opportunities on ThePharmaDaily.com, your trusted platform for clinical research, pharmacovigilance, and healthcare careers.
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Sheffield |Oxfordshire :
Witney |Ontario :
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