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Senior Clinical Research Associate
ICON plcClinical Research Associate monitoring oncology clinical trials across Central/East U.S. Engaging with sites, ensuring compliance with regulatory guidelines, and managing study logistics.
Posted 5/23/2026full-timeRemote • Florida, Illinois, North Carolina, Texas • 🇺🇸 United StatesSenior💰 $110,520 - $138,150 per yearWebsite
Tech Stack
Tools & technologiesGoogle Cloud Platform
About the role
Key responsibilities & impact- Lead on clinical trial monitoring tasks requiring technical depth, with a focus on quality and continuous improvement.
- Monitor clinical trial sites to ensure adherence to study protocols, regulatory requirements, and Good Clinical Practice (GCP) standards.
- Conduct site visits to assess site performance, resolve issues, and provide support to ensure successful trial execution.
- Collaborate with cross-functional teams to ensure timely and accurate data collection and reporting.
- Provide training and guidance to site staff and other CRAs to maintain high standards of clinical trial conduct.
- Build and maintain effective relationships with site personnel and stakeholders to facilitate smooth trial operations.
Requirements
What you’ll need- Bachelor's degree in a relevant scientific discipline or healthcare-related field
- Extensive experience as a Clinical Research Associate, with a strong understanding of clinical trial processes and regulatory requirements.
- Proven ability to manage multiple sites and projects simultaneously, with strong organizational and problem-solving skills.
- Expertise in monitoring practices, data integrity, and site management, with proficiency in relevant clinical trial software and tools.
- Excellent communication, interpersonal, and stakeholder management skills, with the ability to influence and drive compliance within a complex environment.
- Ophthalmology experience required
- Willingness to travel as required (approximately 60%)
Benefits
Comp & perks- Various annual leave entitlements
- A range of health insurance offerings to suit you and your family’s needs.
- Competitive retirement planning offerings to maximize savings and plan with confidence for the years ahead.
- Global Employee Assistance Programme, TELUS Health, offering 24-hour access to a global network of over 80,000 independent specialised professionals who are there to support you and your family’s well-being.
- Life assurance
- Flexible country-specific optional benefits, including childcare vouchers, bike purchase schemes, discounted gym memberships, subsidised travel passes, health assessments, among others.
ATS Keywords
✓ Tailor your resumeApplicant Tracking System Keywords
Tip: use these terms in your resume and cover letter to boost ATS matches.
Hard Skills & Tools
clinical trial monitoringdata integritysite managementregulatory requirementsGood Clinical Practice (GCP)clinical trial processesproblem-solvingorganizational skillsmonitoring practicestraining and guidance
Soft Skills
communicationinterpersonal skillsstakeholder managementinfluencecollaborationrelationship buildingcontinuous improvementsupporttimely reportingproject management