Clinical Research Associate

Oversees and monitors clinical trials to ensure protocols, regulatory guidelines, and GCP are followed.

Oversees clinical trials to ensure adherence to protocols, ethics, and regulatory standards.
Acts as a liaison between clinical sites and sponsors.

  • - Monitor study progress and ensure GCP compliance
  • - Verify data accuracy and resolve discrepancies
  • - Train site staff on study protocols
  • - Prepare visit reports and documentation

To apply for this position, click the Apply button below.

Important: Before applying, please compile all the necessary documents — including your CV, certifications, and any other legally required documents — into a single file for upload.

We appreciate your interest in joining our team and look forward to learning more about you!