Clinical Research Associate (CRA) - Remote

Overview

QPS Netherlands B.V. is looking for a Clinical Research Associate to monitor clinical drug studies across various research centers, ensuring compliance with applicable guidelines.

In Short

• Monitor clinical drug studies according to GCP and WMO guidelines.
• Manage studies from site initiation to close-out.
• Communicate with clients and conduct regular site visits.
• Write reports and verify data.
• Check study drug accountability.
• Discuss study progress and issues with site staff.
• Review execution processes, samples, and materials.
• Work independently during site visits.
• Work from home when not traveling.
• Part of a team focused on clinical research.

Requirements

• Several years of prior clinical trials monitoring experience.
• Knowledge of GCP and WMO guidelines.
• Strong communication skills.
• Ability to work independently and as part of a team.
• Experience in report writing and data verification.
• Willingness to travel to research centers.

Benefits

• Competitive salary range.
• Opportunity to work in a growing clinical research department.
• Flexible working conditions, including remote work.
• Engagement with international pharmaceutical and biotechnological companies.