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 domestic travel approximately 30–40% of 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
Domestic travel 30-40%
Team-based environment
Nice-to-have
Positive and growth-oriented mindset
Proactive and solution-oriented approach
Strong interpersonal and communication skills
Goal-oriented and well-organized
Ability to adapt to clinical IT systems
Use of AI tools
Key Requirements
Bachelor’s degree in Life Sciences or related field