Clinical Research Associate: Trial Monitoring & Compliance in Warsaw

OPIS is seeking a Clinical Research Associate to manage and monitor clinical trials in Poland, ensuring adherence to study protocols, ICH-GCP, and applicable regulations. You will conduct site initiation, monitoring, and close-out visits to safeguard data quality and patient safety. With a minimum of 2 years’ CRA experience, you will apply strong knowledge of ICH-GCP and ISO14155, while maintaining excellent English and MS Office skills.