Medical Study Monitor

4 days ago


kwai tsing district, Hong Kong SAR China IQVIA Argentina Full time
Key Responsibilities
  • You will perform site monitoring visits, including selection, initiation, monitoring, and close-out visits, in accordance with contracted scope of work and regulatory requirements.
  • You will work with sites to develop and track subject recruitment plans, adapting them as needed to meet project objectives.
  • You will administer protocol and related study training to assigned sites and maintain regular communication with sites to manage ongoing project expectations and issues.
  • You will evaluate the quality and integrity of study site practices, identifying areas for improvement and escalating quality issues as necessary.
  • You will manage the progress of assigned studies, tracking regulatory submissions and approvals, recruitment and enrollment, case report form (CRF) completion and submission, and data query generation and resolution.


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