Clinical Research Associate Ii

BeOne

Sao Paulo, Brazil
Hybrid
Clinical monitoring process
Site management
Data quality monitoring
The CRA will conduct site visits and function as the site manager

Job Summary

  • The CRA will conduct site visits and function as the site manager.
  • CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines.
  • BeOne is committed to fighting cancer and values teamwork and collaboration.

Matching Summary

The CRA will conduct site visits and function as the site manager.

Skills & Requirements

Must-have

  • Clinical monitoring process
  • Site management
  • Data quality monitoring

Nice-to-have

  • Collaborative relationships
  • Excellent communication skills
  • Mentoring less experienced CRAs

Key Requirements

  • BS/BA in a relevant scientific discipline
  • Minimum of 2+ years of relevant Clinical Operations experience
  • Fluent in English

Work Rights

Not specified

Tailored Resume

Cover Letter