Internship - Clinical Research Associate (cra)

539

Hybrid
Clinical trial site monitoring
Ich-gcp compliance
Microsoft office proficiency
The Clinical Research Associate Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management and monitoring support

Job Summary

  • The Clinical Research Associate Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management and monitoring support.
  • The role provides hands-on exposure to operational execution of clinical trials under close supervision, preparing the trainee for a future CRA role.
  • The position requires active engagement in on-the-job training to build knowledge of clinical trial phases, monitoring processes, and regulatory requirements.

Matching Summary

The Clinical Research Associate Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management and monitoring support.

Skills & Requirements

Must-have

  • Clinical trial site monitoring
  • ICH-GCP compliance
  • Microsoft Office proficiency
  • Clinical trial operations
  • Domestic travel up to 40%

Nice-to-have

  • Positive and growth-oriented mindset
  • Proactive and solution-oriented approach
  • Strong interpersonal communication
  • Team-based work environment
  • Adaptability to clinical IT systems and AI tools

Key Requirements

  • Bachelor’s degree in Life Sciences or related field
  • Fluent in Portuguese and English
  • Ability to travel domestically 30-40%
  • Intern/Co-op employment status

Work Rights

Not specified

Tailored Resume

Cover Letter