Perform and coordinate all aspects of the clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance
Job Summary
Perform and coordinate all aspects of the clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance.
Ensure trial conduct aligns with approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs to guarantee subject rights, well-being, and data reliability.
Maintain regular contact with investigative sites, facilitate communication between sites, client, and project team, and respond to regulatory requirements and audits.
Matching Summary
Perform and coordinate all aspects of the clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance.