CRA II

We are seeking a Clinical Research Associate to join our team at ICON, responsible for overseeing and coordinating clinical trials, ensuring compliance with regulations, and collecting and analyzing critical data.

Requirements

• University degree in medicine, science/lifesciences or nursing
• At least 12 months of independent on-site monitoring experience for a CRO or pharmaceutical company
• Knowledge of ICH-GCP guidelines and the expertise to review and evaluate medical data
• Excellent written and verbal communication in English
• Good social skills enabling you to deal with queries in a timely manner
• Ability to travel as required of the time domestic - fly and drive across the UK

Benefits

• Competitive base salary and performance related incentives
• Health and wellbeing programmes including medical, dental, and vision coverage
• 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