The CRA Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management, monitoring support, and clinical operations
Job Summary
The CRA Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management, monitoring support, and clinical operations.
Under close supervision, the CRA Trainee will support clinical trial activities in compliance with ICH-GCP, local regulatory requirements, and study-specific documents.
This role is designed to provide hands-on exposure to the operational execution of clinical trials, preparing the trainee for a future CRA role.
Matching Summary
The CRA Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management, monitoring support, and clinical operations.
Skills & Requirements
Must-have
Clinical trial site management
ICH-GCP compliance
Microsoft Office Suite
Fluent in Portuguese
Fluent in English
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
Key Requirements
Bachelor’s degree in Life Sciences, Health Sciences, Biology, or related field
Basic understanding of clinical research phases
Basic understanding of ICH-GCP guidelines
Ability to travel domestically approximately 30–40%