Clinical Research Associate I/II-Onco-Wuhan

When our values align, there's no limit to what we can achieve.
 

Key Accountabilities:

Monitoring and Management of Investigator Sites

• Conducts source data verification (SDV) and ensure clinical trials data are submitted to data management in a timely fashion

• Identifies issues that may impact on the conduct of the study and ensure appropriate closure of all issues

• Proactively manages a greater investigator site workload commensurate with experience, so that studies are run efficiently, and key study objectives are met

• Ensures studies are run in line with ICH/GCP, local laws and Client Standard Operating Procedures (SOPs) and procedures

• Ensures patient safety is maintained and all safety issues are reported correctly according to all relevant local and international regulatory requirements

• Informs the Principal Investigator (PI) and site staff of all issues

• Agrees and develops correctiv...

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