The Field Clinical Research Associate (CRA) is responsible for monitoring site data and ensuring compliance with regulatory requirements and Good Clinical Practice
Job Summary
The Field Clinical Research Associate (CRA) is responsible for monitoring site data and ensuring compliance with regulatory requirements and Good Clinical Practice.
Key responsibilities include performing on-site monitoring visits, ensuring accurate inventory of investigational drug, and maintaining high-quality data collection processes.
This role offers a great opportunity to step into a high-impact, high-visibility role on the early team of Transcend Therapeutics.
Matching Summary
The Field Clinical Research Associate (CRA) is responsible for monitoring site data and ensuring compliance with regulatory requirements and Good Clinical Practice.
Skills & Requirements
Must-have
Perform on-site monitoring visits
Ensure site data accuracy
Maintain investigational drug accountability
Ensure patient safety compliance
Communicate trends, risks, and deviations
Nice-to-have
Detail-oriented with big picture focus
Risk-based decision making
Proactive communication and collaboration
Passion for mental health
Key Requirements
Bachelor's degree in life science
4+ years clinical trial experience
2+ years on-site monitoring experience
Experience with risk-based and hybrid monitoring models