Oversee and monitor clinical trial sites to ensure quality, compliance, and patient safety
Serve as primary Sponsor point of contact for investigative sites
Train and motivate site staff and principal investigators on trial goals and patient treatment
Conduct site evaluations, monitoring, training, and site closure with adherence to GCP/ICH and
Manage site engagement strategies, report progress, and measure impact
Ensure data quality and timely safety reporting; participate in risk assessment and site issue

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