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Clinical Research Associate (Level II) responsible for monitoring investigator sites, ensuring compliance with protocols and ICH-GCP guidelines, and managing documentation and communication with stakeholders.
Perform and coordinate all aspects of the clinical monitoring and site management process, ensuring trial compliance with ICH-GCP guidelines and applicable regulations.
Clinical Research Associate (Level II) responsible for performing and coordinating all aspects of clinical monitoring and site management process, conducting remote or on-site visits to assess protocol and regulatory compliance.