Internship - Clinical Research Associate (cra)

med-in.at

Hybrid
Clinical trial site monitoring
Ich-gcp compliance
Microsoft office proficiency
The Clinical Research Associate (CRA) Trainee will participate in a structured training program within Global Clinical Trial Operations Portugal to develop core competencies in clinical trial site management and monitoring support

Job Summary

  • The Clinical Research Associate (CRA) Trainee will participate in a structured training program within Global Clinical Trial Operations Portugal to develop core competencies in clinical trial site management and monitoring support.
  • The role provides hands-on exposure to clinical trial operational execution, preparing the trainee for a future CRA position under close supervision.
  • The trainee will support clinical trial activities in compliance with ICH-GCP, local regulations, and company policies while actively engaging in on-the-job training.

Matching Summary

The Clinical Research Associate (CRA) Trainee will participate in a structured training program within Global Clinical Trial Operations Portugal to develop 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 support
  • Portuguese and English fluency
  • Domestic travel up to 40%

Nice-to-have

  • Positive and growth-oriented mindset
  • Proactive and solution-oriented approach
  • Strong interpersonal communication
  • Goal-oriented and well-organized
  • Team-based work environment

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 status (Fixed Term)

Work Rights

Not specified

Tailored Resume

Cover Letter