Senior Clinical Research Associate

Role Overview:

• Conduct site monitoring for clinical trials in the Netherlands and Belgium.
• Provide oversight, leadership, and guidance to ensure compliance and quality.
• Coordinate with US and EU teams to address site issues and facilitate negotiations.

Key Responsibilities:

• Review monitoring visit reports and conduct co-monitoring evaluations.
• Ensure setup and collection of site ethics documents and contract negotiations.
• Perform qualification, initiation, interim, and close-out visits with proper documentation.

Qualifications:

• BS/BA in life sciences or related field; 2-3 years clinical monitoring experience.
• Strong organizational, analytical, and leadership skills; ability to manage priorities.
• Fluent in Dutch and English; knowledge of ICH GCP and local regulations.