ICON plc is a global contract research organisation serving the healthcare and pharmaceutical industries. Its work spans clinical, consulting, and commercial services that support drug development from early research through post-marketing activities. The company provides solutions including decentralised clinical trials, cardiac safety, early clinical laboratories, medical imaging, regulatory intelligence, and real-world evidence. ICON plc also brings therapeutic expertise to areas such as cardiovascular disease, oncology, internal medicine, cell and gene therapies, and biosimilars, combining data analysis with patient-focused approaches to help advance clinical programmes.
Senior Clinical Research Associate – Phase I Oncology (Remote, United States)
ICON plc is hiring a Senior Clinical Research Associate to monitor sponsor-dedicated Phase I oncology trials remotely from the United States. The role oversees sites, maintains GCP compliance, and supports clinical trial teams.
United States
Arizona
California
Colorado
Utah$110,520 – $138,150 / year
RemoteFull-timeSeniorEnglish RequiredClinical ResearchDescription
- Manage clinical trial activities in line with study protocols, regulations, and industry standards
- Lead monitoring activities with an emphasis on quality and ongoing process improvement
- Evaluate site compliance with protocols, regulatory obligations, and GCP requirements
- Conduct site visits to review performance, address issues, and support effective study delivery
- Partner with cross-functional teams to ensure accurate, timely data collection and reporting
- Train and mentor site personnel and fellow Clinical Research Associates
- Develop and maintain effective working relationships with site teams and key stakeholders
- Support sponsor-dedicated Phase I oncology studies
Requirements
- Bachelor’s degree in a relevant scientific or healthcare discipline
- Substantial experience working as a Clinical Research Associate
- Thorough knowledge of clinical trial procedures and regulatory requirements
- Demonstrated ability to manage multiple sites and projects concurrently
- Strong organizational, analytical, and problem-solving capabilities
- Advanced knowledge of monitoring procedures, data integrity, and site management
- Proficiency with relevant clinical trial software and tools
- Excellent communication, interpersonal, and stakeholder management abilities
- Availability to travel as needed, approximately 60%
- Current experience monitoring oncology studies
- Legal authorization to work in the country where the role is based
Benefits
- Competitive base pay with performance-linked incentives
- Health and wellbeing programs, including medical, dental, and vision coverage where applicable
- Retirement and pension plans
- Life insurance and disability coverage
- Employee assistance programs and wellbeing resources
- Structured training, learning, and career development opportunities