Clinical Research Associate - sponsor dedicated - Amsterdam
Hybrid · Amsterdam, North Holland, The Netherlands or Utrecht, Utrecht, The Netherlands
Job Summary
You will contribute to clinical trial monitoring activities, including site qualification, initiation, monitoring, and close-out visits, ensuring protocol compliance, data integrity, and patient safety. You’ll collaborate with investigators and site staff, perform data review and resolution of queries to maintain high-quality data, and assist in the preparation and review of study documentation such as protocols and clinical study reports. The role requires 60% travel and fluency in Dutch and English.
Required Qualifications
- 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
- Ability to work independently and collaboratively in a fast-paced environment
- Willingness to travel as required (approximately 60%)
- Fluently in Dutch and English
Additional Requirements
- legal right to work in the country where the role is based
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