Clinical Research Associate (all Level)

BeiGene

Japan, Japan
Ich guidelines and gcp
Clinical trial site contract and budget negotiation
Protocol and related study training
The CRA executes clinical trial protocols at clinical trial sites and monitors clinical trials by ICH guidelines and GCP, local regulations, and applicable SOPs

Job Summary

  • The CRA executes clinical trial protocols at clinical trial sites and monitors clinical trials by ICH guidelines and GCP, local regulations, and applicable SOPs.
  • BeOne is a global oncology company that is discovering and developing innovative treatments that are more affordable and accessible to cancer patients worldwide.
  • Market competitive compensation package including performance-based annual bonus scheme, company shares, and a fantastic benefits program.

Matching Summary

The CRA executes clinical trial protocols at clinical trial sites and monitors clinical trials by ICH guidelines and GCP, local regulations, and applicable SOPs.

Skills & Requirements

Must-have

  • ICH guidelines and GCP
  • clinical trial site contract and budget negotiation
  • protocol and related study training
  • quality and integrity of site practices
  • Trial Master Files (TMFs)
  • risk management process

Nice-to-have

  • highly motivated
  • collaborative
  • passionate interest in fighting cancer
  • proactively identify potential issues
  • seek improvement
  • take initiative for issue resolution

Key Requirements

  • BS in a relevant scientific discipline
  • at least 3 years monitoring experience
  • experience in oncology global trials preferred
  • Fluent in English (writing and speaking)
  • up to 40-70% travel

Work Rights

Not specified

Tailored Resume

Cover Letter