CRC Associate

Role Overview

As a CRC Associate at ICON, you will support clinical research activities to ensure high-quality data, protocol adherence, and patient safety. You will contribute to clinical coordination activities, taking responsibility for your deliverables and working collaboratively.

What You Will Do

Key responsibilities include supporting the setup, coordination, and day-to-day conduct of clinical studies, assisting with patient screening and enrolment, and ensuring accurate completion of source documents and electronic case report forms.

Why It Might Be a Fit

You will bring relevant clinical coordination experience, along with a strong understanding of clinical trial processes, GCP guidelines, and regulatory requirements, and a commitment to data quality and patient safety.

Requirements

• Bachelor's degree in life sciences, nursing, pharmacy, or a related discipline, or equivalent experience in a clinical or healthcare setting
• Initial experience in clinical research or a similar regulated environment
• Basic understanding of clinical trial processes, GCP guidelines, and regulatory requirements
• Strong organisational skills with the ability to manage multiple tasks, priorities, and deadlines with accuracy
• High level of attention to detail and commitment to data quality and patient safety
• Effective communication and interpersonal skills, with the ability to work collaboratively with site staff and cross-functional teams

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage where applicable
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources
• Learning and development opportunities through structured training and career pathways