Clinical Research Associate/臨床開発モニター(東京・大阪・在宅可)

Parexel

Tokyo, Japan
Cra experience of 1 year or more
Gcp compliance
Monitoring clinical trials
At Parexel, we aim to improve the world's health through clinical trials and regulatory consulting

Job Summary

  • At Parexel, we aim to improve the world's health through clinical trials and regulatory consulting.
  • The Clinical Research Associate ensures patient rights and safety while collecting effective scientific data.
  • We value empathy and commitment to making a difference in clinical development.

Matching Summary

At Parexel, we aim to improve the world's health through clinical trials and regulatory consulting.

Skills & Requirements

Must-have

  • CRA experience of 1 year or more
  • GCP compliance
  • monitoring clinical trials

Nice-to-have

  • teamwork skills
  • relationship building
  • flexible decision making

Key Requirements

  • experience in oncology preferred
  • global trial experience desired

Work Rights

Not specified

Tailored Resume

Cover Letter