CRA II

A CRA II at ICON will design and analyze clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies. Key responsibilities include conducting site qualification, initiation, monitoring, and close-out visits for clinical trials.

Requirements

• Bachelor's degree in a scientific or healthcare-related field.
• Minimum of 1.5-2 years of experience as a Clinical Research Associate within CRO/Pharma (mandatory)
• In-depth knowledge of clinical trial processes, regulations, and ICH-GCP guidelines.
• Strong organizational and communication skills, with attention to detail.
• Ability to work independently and collaboratively in a fast-paced environment.
• Willingness to travel as required

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