Clinical Trial Associate
On-site · Utrecht, Utrecht, The Netherlands
Utrecht, Utrecht, The NetherlandsOn-siteFull TimeMid LevelBachelors DegreeEnterprise
Type
Full Time
Level
Mid Level
Education
Bachelors Degree
Company size
Enterprise
Job Summary
Assist in the coordination and administration of clinical trials, ensuring compliance with protocols and regulatory requirements. Maintain and organize study files, essential documents, and regulatory submissions. Support preparation of informed consent forms and case report forms. Work with cross-functional teams to facilitate communication and ensure smooth trial execution. Contribute to tracking and reporting of clinical trial metrics and milestones.
Required Qualifications
- Bachelor's degree in a scientific or healthcare-related field
- Prior experience or strong interest in clinical research
- Knowledge of clinical trial processes, regulations, and guidelines
- Excellent organizational and communication skills
- Ability to work collaboratively in a fast-paced environment with attention to detail
- Willingness to travel as required (approximately 10%)
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