Clinical Research Associate Ii

BeiGene

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, responsible for building and maintaining relationships with key site personnel

Job Summary

  • The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager, responsible for building and maintaining relationships with key site personnel.
  • CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs, monitoring data quality and patient safety.
  • The company seeks motivated, collaborative professionals who share a passionate interest in fighting cancer.

Matching Summary

The CRA will conduct site visits (i.e., PSSV, SIV, IMV, COV) and function as the site manager, responsible for building and maintaining relationships with key site personnel.

Skills & Requirements

Must-have

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

Nice-to-have

  • collaborative spirit
  • entrepreneurial mindset
  • continuous learning
  • Spanish is a plus
  • disease indication training

Key Requirements

  • BS/BA in relevant scientific discipline
  • 2+ years clinical operations experience
  • 1+ years monitoring experience
  • Global oncology trials experience preferred

Work Rights

Not specified

Tailored Resume

Cover Letter