Clinical Research Associate Ii

Nerdgigs

São Paulo, Brazil
Hybrid
Ich-gcp compliance
Clinical trial management systems (ctms)
Electronic trial master files (etmf)
Nerdgigs is seeking a Clinical Research Associate II to join their team in São Paulo or Porto Alegre, Brazil. This hybrid role involves managing relationships with study sites, ensuring compliance with clinical research regulations, and contributing to the success of clinical trials

Job Summary

  • You will be the primary site contact throughout all phases of clinical research studies, ensuring compliance with regulations and contributing to the success of our clinical trials.
  • Conduct remote and on-site monitoring to ensure data integrity and subject safety, documenting findings accurately during site visits.
  • Manage information in Clinical Trial Management Systems (CTMS) and electronic Trial Master Files (eTMF) and act as a Subject Matter Expert (SME) to share best practices and provide training.

Matching Summary

Match Score: 85

Nerdgigs is seeking a Clinical Research Associate II to join their team in São Paulo or Porto Alegre, Brazil. This hybrid role involves managing relationships with study sites, ensuring compliance with clinical research regulations, and contributing to the success of clinical trials.

Skills & Requirements

Must-have

  • ICH-GCP compliance
  • Clinical Trial Management Systems (CTMS)
  • electronic Trial Master Files (eTMF)
  • site selection and validation
  • remote and on-site monitoring
  • regulatory documentation review

Nice-to-have

  • Subject Matter Expert (SME)
  • best practices sharing
  • audit and inspection support
  • continuous improvement

Key Requirements

  • Bachelor’s degree
  • Solid experience as a Clinical Research Associate
  • Fluent in local languages
  • Advanced proficiency in English
  • Valid Driving License

Work Rights

Not specified

Tailored Resume

Cover Letter