Clinical Research Associate

BeiGene

Remote
Clinical monitoring activities
Ich guidelines and gcp
Oncology/hematology clinical 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

  • Clinical monitoring activities
  • ICH guidelines and GCP
  • Oncology/hematology clinical trials
  • Site selection and initiation
  • Data quality and integrity
  • Fluent in English & Turkish

Nice-to-have

  • Collaborative and motivated professionals
  • Passionate interest in fighting cancer
  • Question status-quo and promote innovation
  • SSU experience

Key Requirements

  • BS in a relevant scientific discipline
  • Minimum of 2 years of monitoring experience
  • At least 2 years of CRA monitoring experience
  • Experience in oncology global trials preferred
  • Fluent in English & Turkish

Work Rights

Not specified

Tailored Resume

Cover Letter