CRC Level 1

• Assisting in the coordination and implementation of clinical trial activities under the guidance of Clinical Research Coordinators (CRCs), including patient recruitment, screening, and enrollment.
• Supporting the maintenance and organization of study documentation and regulatory files, ensuring compliance with protocol requirements and regulatory standards.
• Collecting, recording, and entering data into study databases and electronic data capture (EDC) systems, in accordance with study protocols and standard operating procedures (SOPs).
• Assisting with the preparation and submission of regulatory documents and correspondence to regulatory authorities and institutional review boards (IRBs).
• Providing logistical support for study visits, meetings, and other research-related activities, including scheduling appointments, arranging travel, and coordinating study materials.

• Bachelor’s degree in life sciences, healthcare, or related field; relevant experience may be considered in lieu of a degree.
• Previous experience in clinical research or healthcare setting is preferred but Nt required.
• Strong organizational skills and attention to detail, with the ability to manage multiple tasks and priorities effectively.
• Excellent communication and interpersonal skills, with the ability to interact professionally with study participants and colleagues.
• Proficiency in Microsoft Office suite (Word, Excel, Outlook) and willingness to learn new software applications as needed.

Our success depends on the quality of our people. That’s why we’ve made it a priority to build a diverse culture that rewards high performance and nurtures talent.

In addition to your competitive salary, ICON offers a range of additional benefits. Our benefits are designed to be competitive within each country and are focused on well-being and work life balance opportunities for you and your family.

Our benefits examples include:

• 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, LifeWorks, offering 24-hour access to a global network of over 80,000 independent specialized 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, subsidized travel passes, health assessments, among others.

ICON plc is a world-leading healthcare intelligence and clinical research organization. We’re proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.

This role is with Accellacare (https://www.accellacare.com/about) , part of ICON’s clinical research network, where you’ll play a key role in transforming the clinical trial experience for patients and sponsors alike. Our global site network is designed with one goal in mind: to deliver better access, greater efficiency, and improved outcomes in clinical research.

As a CRC Level 1 at ICON, you will design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies.