Clinical Research Associate II

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...

Ready to Apply?

Submit your application today and join our talented team at Parexel.