Clinical Research Associate – Oncology | West Region (Phoenix, Los Angeles, Las Vegas)
Locations: Los Angeles | Las Vegas | Phoenix
Job Reference: JR144441
Company: ICON plc
Division: ICON Strategic Solutions
Department: Clinical Monitoring
Work Model: Remote (Regional Travel Required – West US)
Job Overview
ICON Strategic Solutions is hiring an experienced Clinical Research Associate (CRA) – Oncology to support clinical trial monitoring activities across the West Region of the United States. This position is ideal for professionals based near major hub airports in Phoenix, Los Angeles, or Las Vegas to facilitate regional travel.
The CRA will play a critical role in ensuring site compliance, data integrity, patient safety, and regulatory adherence across oncology clinical trials, including prostate cancer, lung cancer, and hematology studies. This role requires strong therapeutic expertise, proactive site management capabilities, and the ability to maintain inspection readiness in accordance with ICH-GCP and FDA regulations.
Key Responsibilities
Serve as the primary liaison between investigational sites and the sponsor
Conduct all monitoring visit types: Site Selection, Site Initiation, Routine Monitoring, and Close-Out Visits
Ensure compliance with ICH-GCP, FDA regulations, and sponsor SOPs
Maintain accurate documentation in CTMS and eTMF systems
Monitor patient safety, ensuring timely reporting of AEs, SAEs, and PQCs
Support subject recruitment and retention strategies
Oversee investigational product accountability, storage, return, and destruction
Review source documentation and resolve data queries to ensure high-quality data
Track site performance metrics and escalate risks proactively
Collaborate with Clinical Trial Assistants (CTAs), Local Trial Managers (LTMs), and Clinical Trial Managers (CTMs)
Support site budget tracking and payment processes, where applicable
Required Experience
Minimum 2+ years of on-site monitoring experience within a pharmaceutical company or CRO environment
Demonstrated experience in oncology clinical trials, preferably in prostate cancer, lung cancer, or hematology
Strong working knowledge of ICH-GCP, FDA regulations, and US clinical trial requirements
Hands-on experience with CTMS, eTMF, and electronic data capture (EDC) systems
Experience managing multiple investigative sites independently
Educational Qualifications
Bachelor’s degree in Life Sciences, Pharmacy, Nursing, or a related scientific discipline preferred
Registered Nurse (RN) qualification may be considered in lieu of a life sciences degree
Eligibility & Travel Requirements
Must be legally authorized to work in the United States without visa sponsorship
Willingness to travel up to 50% for on-site monitoring visits across the West Region
Candidates residing near major airports in Phoenix, Los Angeles, or Las Vegas strongly preferred
Core Competencies
Strong clinical monitoring and site management expertise
High attention to detail and quality compliance mindset
Effective problem-solving and risk mitigation skills
Excellent communication and stakeholder management abilities
Ability to manage multiple protocols and timelines simultaneously
Why Join ICON plc?
ICON plc is a leading global clinical research organization delivering outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies worldwide. ICON is recognized for operational excellence, regulatory expertise, and innovation in clinical development.
Employees benefit from:
Competitive compensation package
Comprehensive health insurance options
Retirement planning programs
Generous annual leave policies
Global Employee Assistance Programme (LifeWorks)
Life assurance coverage
Flexible, country-specific benefits supporting work-life balance
ICON is committed to diversity, inclusion, and equal employment opportunity, fostering a collaborative environment that supports career advancement in clinical research.
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