Instagram
youtube
Facebook

Senior Cra - Oncology - Midwest

2+ years
Not Disclosed
10 April 18, 2025
Job Description
Job Type: Full Time Remote Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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:

Senior CRA – Oncology (Midwest)


Location:

United States (Remote – Midwest region preferred)


Job ID:

2025-118002


Department:

Clinical Monitoring – ICON Strategic Solutions


Job Type:

Full-Time, Remote


Application Contact:

Name: Jamie Pruitt
Options: View other roles or send a direct message through the platform


Job Description:

As a Senior Clinical Research Associate (CRA) in Oncology, you will support clinical trials from site evaluation through closeout, ensuring compliance, data integrity, and regulatory adherence. Your focus will be on early- to late-phase oncology trials across the Midwest region. Oncology monitoring experience is required.


Key Responsibilities:

  • Evaluate, initiate, monitor, and close out clinical trial sites

  • Ensure compliance with protocols, ICH/GCP, SOPs, and regulatory requirements

  • Serve as the primary liaison for site personnel

  • Provide site training on protocols, systems, and procedures

  • Support recruitment strategies and subject safety

  • Monitor and ensure data quality and timely entry into EDC systems

  • Resolve site performance issues and implement corrective actions

  • Maintain audit-ready trial documentation and site files

  • Verify investigational product handling, compliance, and availability

  • Develop and sustain strong site relationships throughout the study

  • Travel 8–10 days/month to clinical trial sites


Requirements:

  • Education:

    • BA/BS in Life Sciences or equivalent; RN acceptable

  • Experience:

    • Minimum 2+ years of CRA experience (pharma/biotech industry)

    • Must have oncology monitoring experience (Phases I–III)

    • Knowledge of GCP, FDA CFR, ICH, HIPAA, and local regulatory guidelines

    • Proficient in EDC, IVRS, CTMS, and Microsoft Office

    • Strong communication, time management, problem-solving, and project planning skills

    • Must possess a valid driver’s license

    • Willingness to travel regionally


Benefits:

  • Competitive salary with performance-based rewards

  • Annual leave entitlements

  • Customizable health insurance plans for you and your family

  • Robust retirement savings options

  • TELUS Health 24/7 employee support network

  • Life assurance

  • Additional perks (gym discounts, bike schemes, travel passes, etc.)
    🔗
    Explore ICON Benefits


Inclusion & Accessibility:

ICON is an equal opportunity employer committed to diversity, inclusion, and accessible hiring processes.
🔗
Request accommodations here