In-House Clinical Research Associate
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Job Summary
Assisting with operational activities in clinical studies, the full-time In-House Clinical Research Associate will support site management and monitoring tasks, ensuring compliance with protocols and regulatory requirements while working in a hybrid environment.
Key responsibilities
- Collects, reviews, and maintains essential documents, ensuring compliance with good documentation practices
- Communicates effectively with internal project staff and site personnel to address questions and track trial progress
- Assists in audit preparation and may support the CRA during monitoring visits and site activation processes
Required qualifications
- Bachelor's Degree in a scientific discipline is required
- Less than 1 year of previous clinical research experience is preferred
- Proficiency in MS Office Suite is essential
- Strong organizational skills and attention to detail are required
- Ability to work collaboratively in a team-oriented environment with minimal oversight is necessary
Complete Job Description
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