Clinical Research Associate Ii

29

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

Job Summary

  • This role serves as the primary site contact throughout all phases of clinical research studies to ensure regulatory compliance.
  • The successful candidate will conduct remote and on-site monitoring to guarantee data integrity and subject safety.
  • Candidates must possess strong communication skills to effectively coordinate with investigators and resolve site performance issues.

Matching Summary

This 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 knowledge
  • Site management and monitoring experience
  • Fluent in English and local languages
  • CTMS and eTMF proficiency

Nice-to-have

  • Subject Matter Expertise capability
  • Strong analytical skills for data metrics
  • Ability to work independently in fast-paced environment
  • Experience with audit and inspection activities

Key Requirements

  • Bachelor's degree
  • Solid Clinical Research Associate experience
  • Valid driving license not required but travel is 75%
  • No VISA sponsorship available

Work Rights

Local candidates preferred (São Paulo or Porto Alegre)

Tailored Resume

Cover Letter