Clinical Research Associate

Job Summary

To support clinical studies in Belgium, the full-time remote Clinical Research Associate will manage site evaluations, monitor compliance, and ensure data quality while fostering relationships with investigators and site teams.

Key responsibilities

• Serve as the primary contact for investigative sites, coordinating study information and internal stakeholder communication
• Conduct site evaluations, initiation, monitoring, and close-out activities in compliance with protocols and regulations
• Develop site engagement strategies and perform ongoing risk assessments to ensure participant safety and study performance

Required qualifications

• Degree or equivalent qualification in a health-related discipline, such as Medicine, Life Sciences, or Nursing
• At least one year of clinically related experience, including six months in clinical research monitoring
• Familiarity with risk-based monitoring approaches and knowledge of relevant therapeutic areas
• Fluency in French, Dutch, and English
• Strong planning and organizational skills with the ability to manage competing priorities