Internship - Clinical Research Associate (cra)

leHACK

Hybrid
Clinical trial site management
Ich-gcp compliance
On-site and remote monitoring
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.
  • This role provides hands-on exposure to clinical trial operational execution under close supervision, preparing the trainee for a future CRA role.
  • The position requires active engagement in on-the-job training and the ability to travel domestically approximately 30–40% of the working time for training and site support.

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 management
  • ICH-GCP compliance
  • On-site and remote monitoring
  • Microsoft Office proficiency
  • Clinical IT systems adaptability
  • Domestic travel up to 40%

Nice-to-have

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

Key Requirements

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

Work Rights

Not specified

Tailored Resume

Cover Letter