Clinical Trial Associate

ICON plc is a global healthcare intelligence and clinical research organization seeking a Clinical Trial Associate (CTA) to join its team. The role supports site-level execution of clinical trials by overseeing site management activities and ensuring regulatory and operational compliance. You will collaborate with clinical teams and site staff to deliver high-quality data and meet study 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 ensure 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 and support process improvement.
• Prepare and maintain site management documentation, including site reports, communications, and site performance updates.

• 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.

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

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

• Competitive salary (amount not specified).

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

• Inclusive workplace with reasonable accommodation available during the application process.