Clinical Research Associate Ii

beigene.ae

Sao Paulo, Brazil
Hybrid
Ich-gcp guidelines
Site visits
Data quality
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.
  • CRAs are to complete all aspects of the clinical monitoring process in accordance with ICH-GCP guidelines, local regulations, and applicable SOPs.
  • Provides site level management for established protocols and portfolio under general supervision.

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
  • patient safety
  • Fluent English

Nice-to-have

  • collaborative Spirit
  • driving Excellence
  • entrepreneurial Mindset
  • analytical Thinking/Data Analysis
  • Spanish is a plus

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter