About this role
About the Role ICON is seeking a Clinical Research Associate II (CRA II) with prior monitoring experience to support the design, analysis, and oversight of clinical trials. You will contribute to advancing innovative treatments while ensuring patient safety and high-quality data across trial sites. What You'll 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.
- Perform data review and resolution of queries to maintain high-quality clinical data.
- Contribute to the preparation and review of study documentation, including protocols and clinical study reports. What We're Looking For
- 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 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 (approximately 60%). Compensation & Benefits
- Competitive salary and a range of benefits focused on well-being and work-life balance.
- Annual leave entitlements and health insurance offerings.
- Competitive retirement planning options.
- Global Employee Assistance Programme (LifeWorks) with 24-hour access to a network of professionals.
- Life assurance and flexible country-specific benefits (e.g., childcare vouchers, bike purchase schemes, gym discounts, travel subsidies, health assessments).