Sr CRA

As a Clinical Research Associate (CRA) at ICON, you will contribute to our clinical trial operations function, working collaboratively to deliver high-quality outcomes across our clinical programs. You will work independently and actively to coordinate all activities for setting up and monitoring a study, completing accurate study status reports and maintaining study documentation. Your role will involve delivering clinical trial monitoring work to a high standard, working closely with your team and stakeholders.

Requirements

• University degree in medicine, science, or equivalent
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Experience monitoring Oncology studies
• Good social skills enabling you to deal with queries in a timely manner
• Willingness to travel as required (approximately 60%)

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