Clinical Research Associate Ii

539

São Paulo, Brazil
Hybrid
Bachelor's degree required
Ich-gcp and local regulations compliance
Remote and on-site clinical monitoring
The role serves as the primary site contact throughout all phases of clinical research studies to ensure regulatory compliance

Job Summary

  • The role serves as the primary site contact throughout all phases of clinical research studies to ensure regulatory compliance.
  • Candidates will conduct remote and on-site monitoring to maintain data integrity and subject safety while documenting findings accurately.
  • This position requires managing information in Clinical Trial Management Systems and acting as a Subject Matter Expert to share best practices.

Matching Summary

The role serves as the primary site contact throughout all phases of clinical research studies to ensure regulatory compliance.

Skills & Requirements

Must-have

  • Bachelor's degree required
  • ICH-GCP and local regulations compliance
  • Remote and on-site clinical monitoring
  • Site management and relationship building
  • Protocol adherence and data integrity

Nice-to-have

  • Strong analytical skills for data metrics
  • Ability to work independently in fast-paced environment
  • Experience with CTMS and eTMF systems
  • Subject Matter Expertise for training others
  • Fluency in local languages and advanced English

Key Requirements

  • Bachelor's degree
  • Solid experience as a Clinical Research Associate
  • Proficiency in MS Office and clinical IT applications

Work Rights

Not specified

Tailored Resume

Cover Letter