Overview

ICON plc is a leading healthcare intelligence and clinical research organization dedicated to shaping the future of clinical development. We invite you to join our mission.

Responsibilities

• Monitor clinical trial sites for adherence to protocols and GCP standards.
• Conduct site visits for performance assessment and issue resolution.
• Collaborate with teams for accurate data collection.
• Train site staff and CRAs to uphold trial conduct standards.
• Maintain relationships with stakeholders for smooth operations.

Your Profile

• Advanced degree in life sciences, nursing, or medicine.
• Extensive experience as a Clinical Research Associate.
• Strong organizational skills with the ability to manage multiple projects.
• Expertise in monitoring, data integrity, and site management.
• Excellent communication and interpersonal skills.

What ICON Offers

We prioritize a diverse culture and offer competitive salaries along with benefits designed for your well-being and work-life balance.

Benefits Include

• Annual leave entitlements.
• Health insurance options.
• Retirement planning benefits.
• 24-hour access to Employee Assistance Programme.
• Flexible optional benefits.

Inclusion & Accessibility

At ICON, we are committed to providing an inclusive environment free from discrimination. All qualified applicants are encouraged to apply.

Interested Candidates

If you're interested but unsure about meeting all requirements, we encourage you to apply as you may be the perfect fit for ICON.