Support and observe in-house clinical site monitoring and site management for full-service studies.
Ensure protocol, SOP and regulatory compliance across sites.
Drive investigative sites and patient recruitment, ensuring compliance and oversight.
Conduct remote data review and assist with data queries and closure.
Support RBM activities; assess data collection and regulatory documents.
Perform remote activities for investigational sites per ICH GCP standards.

🎯 Requirements

Undergraduate degree (Bachelor or Honors) and 1-3 years' related experience.
Training in clinical research and site monitoring is a plus.

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