Clinical Research Associate Ii

Beonemedicines Com Au

Sao Paulo, Brazil
Hybrid
Ich-gcp guidelines
Site visits (pssv, siv, imv, cov)
Data quality and patient safety monitoring
The CRA will assume the role of a primary CRA, conducting site visits and functioning as the site manager to build and maintain relationships with key site personnel

Job Summary

  • The CRA will assume the role of a primary CRA, conducting site visits and functioning as the site manager to build and maintain relationships with key site personnel.
  • CRAs are responsible for monitoring data quality and patient safety through monitoring and site education, ensuring compliance with ICH-GCP guidelines, local regulations, and SOPs.
  • The company seeks highly motivated, collaborative professionals with a passionate interest in fighting cancer, offering challenging and exciting opportunities.

Matching Summary

The CRA will assume the role of a primary CRA, conducting site visits and functioning as the site manager to build and maintain relationships with key site personnel.

Skills & Requirements

Must-have

  • ICH-GCP guidelines
  • site visits (PSSV, SIV, IMV, COV)
  • data quality and patient safety monitoring
  • Fluent English required

Nice-to-have

  • collaborative spirit
  • scientific and business professionals
  • passionate interest in fighting cancer
  • Spanish is a plus

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter