Perform and coordinate different aspects of the clinical monitoring and site management process
Job Summary
Perform and coordinate different aspects of the clinical monitoring and site management process.
Conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
Ensure that the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subjects' rights, well-being, and data reliability.
Matching Summary
Perform and coordinate different aspects of the clinical monitoring and site management process.