Clinical Research Associate - FSP - Remote

Role Overview:

• As a CRA II at ICON, you will design and analyze clinical trials, interpreting complex medical data.
• You will contribute to clinical trial monitoring activities, taking responsibility for your deliverables.
• Work collaboratively with a global team dedicated to advancing innovative treatments.

What You Will Do:

• Conduct site qualification, initiation, monitoring, and close-out visits for clinical trials.
• Ensure protocol compliance, data integrity, and patient safety throughout the trial process.
• Collaborate with investigators and site staff to facilitate smooth study conduct.

Your Profile:

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 2 years of experience as a Clinical Research Associate.
• In-depth knowledge of ICH-GCP guidelines and regulatory requirements.

Rewards & Benefits:

• Competitive base salary and performance-related incentives.
• Health and wellbeing programs including medical, dental, and vision coverage.
• Retirement and pension plans, life assurance, and disability coverage.