About this role
About the Role ICON plc is a world-leading healthcare intelligence and clinical research organization. As a Clinical Research Associate, you will contribute to our clinical trial monitoring activities and work collaboratively to deliver high-quality outcomes across our clinical programs. 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 1 year 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.
- Fluency in Dutch and English. Nice to Have
- Experience in therapeutic areas such as diabetes, obesity, or rare blood disorders. Compensation & Benefits
- Competitive salary and a comprehensive benefits package including:
- Various annual leave entitlements
- Health insurance offerings
- Retirement planning opportunities
- LifeWorks (EAP) with 24-hour global support
- Life assurance
- Flexible country-specific optional benefits (e.g., childcare vouchers, bike purchase schemes, gym discounts, travel passes, health assessments)