The Clinical Research Associate Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management and monitoring support
Job Summary
The Clinical Research Associate Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management and monitoring support.
This role provides hands-on exposure to the operational execution of clinical trials 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 Trainee will participate in a structured training program aimed at developing core competencies in clinical trial site management and monitoring support.
Skills & Requirements
Must-have
Clinical trial site monitoring
ICH-GCP compliance
Microsoft Office proficiency
Domestic travel up to 40%
Clinical IT systems adaptability
Nice-to-have
Positive and growth-oriented mindset
Proactive and solution-oriented approach
Strong interpersonal communication skills
Goal-oriented and well-organized
Team-based work environment
Key Requirements
Bachelor’s degree in Life Sciences or related field