Clinical Trial Associate

ICON plc is a healthcare intelligence and clinical research organization seeking a Clinical Trial Associate (CTA) to support site-level execution of clinical trials. The role focuses on overseeing site management activities to ensure regulatory compliance, high-quality data, and achievement of study timelines and goals.

• Oversee day-to-day site management activities to ensure compliance with study protocols, regulatory requirements, and timelines.
• Collaborate with site staff and cross-functional teams to resolve issues, monitor progress, and support timely data collection and reporting.
• Assist with site initiation, monitoring visits, and close-out activities to support proper trial execution.
• Provide guidance and mentorship to junior site management staff to foster collaboration and process improvement.
• Prepare and maintain site management documentation, including site reports, communications, and updates on site performance.

• Bachelor’s degree in life sciences, clinical research, or a related field.

• Extensive experience in site management, clinical operations, or monitoring within the clinical research industry.

• Strong understanding of clinical trial processes, Good Clinical Practice (GCP), and regulatory requirements.

• Strong problem-solving and organizational skills, with the ability to manage multiple sites and timelines.

• Effective communication and interpersonal skills with a collaborative approach and ability to maintain strong site relationships.

• Competitive salary (amount not specified).

• Benefits may include annual leave entitlements, health insurance options, retirement planning, Employee Assistance Program (LifeWorks), life assurance, and country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, discounted gym memberships, subsidized travel passes, health assessments).

• Inclusive and accessible workplace; reasonable accommodations available during the application process.