Clinical Site Associate

Clinical Site Associate at ICON, supporting clinical trial operations, ensuring site compliance, and documentation accuracy.

Requirements

• Bachelor's or Master's degree in life sciences or healthcare
• Previous experience in clinical research (6-18 months)
• Fluency in French and English
• Knowledge of ICH-GCP and clinical trial regulations

Benefits

• Competitive base salary
• Performance related incentives
• Health and wellbeing programmes
• Retirement and pension plans
• Life assurance and disability coverage
• Employee assistance programmes and wellbeing resources