Performs site qualification, site initiation, interim monitoring, site management activities and close-out visits
Uses judgment and experience to evaluate overall performance of site and site staff
Maintains a working knowledge of ICH/GCP Guidelines or other applicable guidance
Verifies the process of obtaining informed consent has been adequately performed
Assesses factors that might affect subject/patient’s safety and clinical data integrity
Supports subject/patient recruitment, retention and awareness strategies

Bachelor’s degree or RN in a related field
Knowledge of Good Clinical Practice/ICH Guidelines and other applicable regulatory requirements
Previous monitoring experience
Must demonstrate good computer skills
Fluency in French and English and a good understanding of Dutch

Clinical Research Associate

Key skills