Clinical Research Associate Ii

Beonemedicines

Sao Paulo, Brazil
Hybrid
Ich-gcp guidelines
Site visits
Data quality monitoring
The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager

Job Summary

  • The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager.
  • The CRA is responsible to build and maintain relationships with key site personnel and ensure an effective line of communication.
  • CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.

Matching Summary

The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager.

Skills & Requirements

Must-have

  • ICH-GCP guidelines
  • site visits
  • data quality monitoring
  • patient safety monitoring
  • Fluent English required

Nice-to-have

  • collaborative Spirit
  • Fighting cancer
  • scientific professionals
  • business professionals
  • Spanish is a plus

Key Requirements

  • BS/BA in relevant scientific discipline
  • 2+ years Clinical Operations experience
  • 1+ years monitoring experience
  • Experience in global oncology trials preferred

Work Rights

Not specified

Tailored Resume

Cover Letter