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Senior Cra - Oncology - West Coast

5+ years
$110,520/year – $138,150/year USD
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 Clinical Research Associate – Oncology – West Coast


Location:

United States (Remote – Candidates must reside in the Western U.S., especially California and surrounding states)


Job ID:

2025-116313


Department:

Clinical Monitoring (ICON Strategic Solutions)


Job Type:

Full-Time, Remote


Application Contact:

Name: Jamie Pruitt
Message Option: Available via the job platform
View Roles: See Jamie’s other open roles


Job Description:

About ICON:
ICON plc is a world-leading healthcare intelligence and clinical research organization focused on innovation and excellence. ICON fosters an inclusive, diverse, and high-performance culture that rewards talent and dedication.


Key Responsibilities:

  • Perform all phases of site management for Oncology studies (qualification, initiation, monitoring, close-out)

  • Serve as the primary point of contact between sites and the clinical trial team

  • Ensure continuous inspection readiness at assigned sites

  • Document monitoring activities and submit visit reports promptly

  • Support document collection and TMF reconciliation

  • Guide sites through IRB/EC submissions and confirm approvals

  • Monitor Key Risk Indicators (KRIs) and resolve issues proactively

  • Independently create and implement CAPA plans

  • Train site staff in GCP, SOPs, and study protocols

  • Assist sites during regulatory inspections

  • Contribute to site feasibility, qualification, and activation

  • Lead site engagement activities, especially for Oncology-focused sites


Qualifications & Experience:

  • Education:

    • Bachelor’s degree in a scientific or healthcare-related field preferred

  • Experience:

    • Minimum 5+ years of independent Oncology clinical monitoring experience

    • 1+ year of early development trial experience

    • Solid tumor trial monitoring experience preferred

    • Familiarity with Veeva systems preferred

    • Prior experience training site staff and supporting regulatory inspections

    • Experience with Risk-Based Monitoring and working in FSP or in-house models

  • Location Requirement:

    • Must reside in the Western USA (ideally California or neighboring states)

    • Travel: Up to 50% domestic travel required


Salary Range:

$110,520/year – $138,150/year USD
(Exact compensation based on experience, education, and location)


ICON Employee Benefits Include:

  • Competitive leave policies

  • Multiple health insurance plan options for employees and families

  • Retirement planning with employer contributions

  • Global Employee Assistance Program via TELUS Health

  • Life insurance and country-specific optional perks like:

    • Gym memberships

    • Bike-to-work programs

    • Travel subsidies

    • Health checks

    • Childcare vouchers

🔗 More benefits: ICON Careers – Benefits


Diversity & Accessibility Statement:

ICON is committed to creating a diverse, inclusive, and discrimination-free workplace. All qualified candidates will be considered.
🔗
Request reasonable accommodation