Clinical Research Associate

🕒 May 20

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ICON plc

WebsiteLinkedInAll Job Openings

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕️ Healthcare Insurance

Pharmaceuticals • Biotechnology • Healthcare Insurance

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

• Monitor clinical trial sites to ensure full compliance with study protocols, regulatory requirements, and Good Clinical Practice (GCP). • Conduct UK site visits to evaluate performance, troubleshoot issues, and support sites in delivering successful study outcomes. • Collaborate with cross‑functional teams to ensure accurate, timely data collection and reporting. • Provide training, mentorship, and guidance to site staff and fellow CRAs to uphold high standards of trial conduct. • Build strong, productive relationships with site personnel and stakeholders to ensure smooth study operations.

🎯 Requirements

• Hold an advanced degree in life sciences, nursing, medicine, or a related field. • Bring significant experience as an Oncology CRA, with deep knowledge of clinical trial processes and regulatory frameworks. • Demonstrate the ability to manage multiple sites and projects with strong organisational and problem‑solving skills. • Possess expertise in monitoring, site management, and data quality, with proficiency in clinical trial systems and tools. • Communicate confidently and effectively, with strong interpersonal and stakeholder‑management capabilities. • Able to travel to UK sites as required and hold a valid driver’s licence.

🏖️ Benefits

• 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.