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.
The 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.
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 management
ICH-GCP compliance
On-site and remote monitoring
Microsoft Office proficiency
Portuguese and English fluency
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 work environment
Key Requirements
Bachelor’s degree in Life Sciences or related field