Clinical Research Associate

📋 Description

• Serve as the primary point of contact for assigned investigative sites, providing relevant study
• Build effective working relationships with investigators and site staff, and support their
• Conduct site evaluation, initiation, routine monitoring, and close-out activities in accordance
• Support the safety and protection of study participants throughout the clinical trial.
• Develop and adapt site engagement strategies based on study requirements and local site insights
• Apply knowledge of the protocol, scientific principles, therapeutic area, and patient journey to

🎯 Requirements

• Degree or equivalent qualification in a health-related discipline, such as Medicine, Life Sciences
• At least one year of clinically related experience, including a minimum of six months of experience
• Familiarity with risk-based monitoring approaches, including on-site and remote monitoring.
• Knowledge of relevant therapeutic areas and the ability to apply scientific concepts to clinical
• Knowledge of local regulatory and legal requirements, ICH/GCP Guidelines, and applicable policies.
• Fluency in French, Dutch, and English is required.