Clinical Research Associate

Monitor clinical performance evaluations, prepare clinical trial documents, and perform site visits as a Clinical Research Associate.

Requirements

• University degree in biology, medicine, pharmacy or an equivalent combination of education, training and work experience in clinical trials
• At least 2 years of experience as a clinical research associate/ clinical monitor in a CRO/medical device or pharmaceutical company
• Good knowledge of current industry practices related to the conduct of clinical trials (ICH-GCP, ISO14155, ISO 20916)
• Good knowledge of MDR and IVDR, as well as good understanding of GDPR