In-House Clinical Research Associate

Assisting with operational activities for clinical studies, the full-time In-House Clinical Research Associate will support site management and monitoring, ensuring compliance with protocols and regulatory requirements in a remote work environment. Key responsibilities Collects, reviews, and maintains essential documents, ensuring compliance with good documentation practices Communicates and coordinates effectively with internal project staff and site personnel to address inquiries and support trial progress Assists in audit preparation and may support site activation processes and tracking of site training and recruitment efforts Required qualifications Bachelor's Degree in a scientific discipline Less than 1 year of previous clinical research experience preferred Proficiency in MS Office Suite Strong organizational and critical thinking skills Ability to work collaboratively in a team-oriented environment with minimal supervision