The Clinical Research Associate Trainee will participate in a structured training program to develop core competencies in clinical trial site management and monitoring support
Job Summary
The Clinical Research Associate Trainee will participate in a structured training program 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 position.
The position requires domestic travel approximately 30–40% of working time and fluency in both Portuguese and English.
Matching Summary
The Clinical Research Associate Trainee will participate in a structured training program 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 operations support
Domestic travel up to 40%
Fluent Portuguese and English
Nice-to-have
Positive and growth-oriented mindset
Proactive and solution-oriented approach
Strong interpersonal communication
Team-based environment adaptability
Ability to use AI tools
Key Requirements
Bachelor’s degree in Life Sciences or related field