Clinical Research Associate

Beonemedicines Com Au

Ich guidelines and gcp
Clinical trial site monitoring
Oncology/hematology trials
The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs

Job Summary

  • The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.
  • The CRA is responsible for collaborating closely with the Regional Clinical Operations Manager to ensure study timelines are adhered to and required quality standards are maintained.
  • BeOne continues to grow at a rapid pace with challenging and exciting opportunities for experienced professionals.

Matching Summary

The CRA executes clinical monitoring activities at clinical trial sites and monitors clinical trials in accordance with ICH guidelines and GCP, local regulations, and applicable SOPs.

Skills & Requirements

Must-have

  • ICH guidelines and GCP
  • clinical trial site monitoring
  • oncology/hematology trials
  • data query resolution
  • inspection readiness

Nice-to-have

  • scientific and business professionals
  • collaborative spirit
  • question status-quo
  • promote innovation
  • passionate interest in fighting cancer

Key Requirements

  • BS in a relevant scientific discipline
  • minimum of 2 years monitoring experience
  • Fluent in English & Italian
  • at least 2 years CRA monitoring experience

Work Rights

Not specified

Tailored Resume

Cover Letter