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Clinical Data Reviewer

5+ years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Remote Education: MD, PharmD, PhD, Nursing degree, or MS Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

 

Job Title:

Clinical Data Reviewer


Location:

Remote – United States


Job ID:

2025-118608


Department:

Clinical Trial Management – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Jonathan Holmes
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Job Description:

As a Clinical Data Reviewer, you will play a key role in ensuring data accuracy, integrity, and compliance across global clinical trials. You’ll be responsible for reviewing clinical and medical data, identifying inconsistencies, and collaborating with teams to resolve data queries and support study readiness.


Key Responsibilities:

  • Conduct clinical/medical data reviews to identify errors and clarify with study sites

  • Perform trend analysis and targeted data reviews to ensure protocol compliance

  • Communicate training needs to CRAs, sites, and internal teams

  • Support data cleaning and query resolution to maintain audit readiness

  • Participate in review meetings, including:

    • Protocol Deviation Review

    • Data Review and Quality Team (DRQT)

    • Statistical Review of Clinical Data (SRCD)

    • Safety Monitoring Team (SMT)

  • Assist with data capture guidance, narrative preparation, and top-line slide creation


Requirements:

  • Education:

    • MD, PharmD, PhD, Nursing degree, or MS in a scientific field

  • Experience:

    • Minimum 5 years of clinical/medical data review experience (8+ years preferred)

    • Experience with solid tumor oncology is required

    • Clinical cross-checking, coding review, and data query writing experience

    • Proficient in clinical databases, Microsoft Excel, and project management tools

  • Skills:

    • Strong understanding of GCP and clinical trial design

    • Excellent communication, organizational, and analytical skills

    • Demonstrated ability to meet project deadlines and collaborate across teams


Benefits:

  • Competitive salary and annual leave entitlements

  • Comprehensive health insurance options

  • Retirement savings and financial planning support

  • Global Employee Assistance via TELUS Health

  • Life assurance

  • Optional, country-specific perks such as:

    • Childcare vouchers, gym discounts, bike schemes, travel subsidies, and wellness assessments
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      Explore ICON Benefits


Inclusion & Accessibility:

ICON is dedicated to a diverse and inclusive work environment. Accommodations are available for applicants during the hiring process.
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Request accommodations here