The job posting is for a Clinical Research Associate (Level II) position at PPD (Thermo Fisher) in Chengdu, China. The role involves performing clinical monitoring and site management, ensuring compliance with protocols and regulations while maintaining data integrity
Job Summary
As a Clinical Research Associate (Level II), you'll conduct remote or on-site visits to assess protocol and regulatory compliance and manage required documentation.
You will manage procedures and guidelines from different sponsors and/or monitoring environments (i.e., FSO, FSP, Government, etc.).
Ensures subjects' rights, well-being, and data reliability by ensuring the trial is conducted in accordance with the approved protocol, ICH-GCP guidelines, applicable regulations, and SOPs.
Matching Summary
Match Score: 85
The job posting is for a Clinical Research Associate (Level II) position at PPD (Thermo Fisher) in Chengdu, China. The role involves performing clinical monitoring and site management, ensuring compliance with protocols and regulations while maintaining data integrity.
Skills & Requirements
Must-have
Risk-based monitoring approach
ICH-GCP guidelines
Investigational product assessment
Site processes specialist
Data accuracy through SDR, SDV and CRF review
Nice-to-have
Collaborative relationships with investigational sites