Clinical Research Associate – Oncology | Missouri (Remote Monitoring Role)
Location: Missouri
Job Reference: JR144443
Company: ICON plc
Division: ICON Strategic Solutions
Department: Clinical Monitoring
Work Model: Remote (Regional Travel Required)
Job Overview
ICON Strategic Solutions is seeking a dedicated Clinical Research Associate (CRA) – Oncology to manage and monitor oncology clinical trials across Missouri. This role is critical in ensuring clinical trial integrity, regulatory compliance, patient safety, and high-quality data delivery in accordance with ICH-GCP and US regulatory standards.
The CRA will oversee investigational sites, support oncology programs including prostate cancer, lung cancer, and hematology studies, and maintain inspection readiness across all assigned protocols.
This opportunity is ideal for experienced clinical monitors looking to advance their career within a globally recognized clinical research organization.
Key Responsibilities
Act as the primary liaison between investigational sites and the sponsor
Conduct Site Selection, Site Initiation, Routine Monitoring, and Close-Out Visits
Ensure compliance with ICH-GCP, FDA regulations, and sponsor SOPs
Maintain accurate and up-to-date documentation in CTMS and eTMF systems
Monitor patient safety, ensuring timely reporting of AEs, SAEs, and PQCs
Support site recruitment and retention strategies to meet enrollment targets
Oversee investigational product accountability, storage, and reconciliation
Perform source data verification (SDV) and resolve data queries efficiently
Identify, escalate, and mitigate site risks to maintain study timelines
Collaborate with 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 independent on-site monitoring experience within a pharmaceutical company or CRO
Demonstrated experience in oncology clinical trials; exposure to prostate cancer, lung cancer, or hematology studies preferred
Strong working knowledge of ICH-GCP, FDA regulations, and US clinical trial processes
Hands-on experience with CTMS, eTMF, and electronic data capture (EDC) systems
Proven ability to manage multiple sites simultaneously
Educational Qualifications
Bachelor’s degree in Life Sciences, Nursing, Pharmacy, 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 Missouri and surrounding areas
Candidates residing near major Missouri airport hubs preferred for efficient regional travel
Core Competencies
Strong clinical monitoring and regulatory compliance expertise
Excellent problem-solving and risk management skills
High attention to detail and data integrity focus
Strong communication and stakeholder management abilities
Ability to manage competing priorities in a fast-paced environment
Why Join ICON plc?
ICON plc is a leading global clinical research organization providing outsourced development and commercialization services to pharmaceutical, biotechnology, and medical device companies worldwide. ICON supports clinical programs across all phases, ensuring scientific excellence and regulatory compliance.
Employees benefit from:
Competitive salary and performance-driven compensation
Comprehensive health insurance coverage
Retirement savings and financial planning programs
Generous annual leave entitlements
Global Employee Assistance Programme (LifeWorks)
Life assurance coverage
Flexible, country-specific employee benefits
ICON is committed to diversity, inclusion, and equal opportunity employment, fostering an environment where clinical professionals can grow and excel.
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