Clinical Operations Intern

You will be responsible for supporting the clinical operations team with documentation and coordination tasks. Additionally, you will assist in site management activities and trial documentation preparation while ensuring compliance with protocols and regulatory guidelines. It is important for you to learn the fundamentals of Good Clinical Practice (GCP) and regulatory requirements. Your key responsibilities will include: - Supporting the clinical operations team with documentation and coordination tasks - Assisting in site management activities and trial documentation preparation - Ensuring compliance with protocols and regulatory guidelines - Learning the fundamentals of Good Clinical Practice (GCP) and regulatory requirements The qualifications required for this role are: - Strong organizational and time-management skills - Excellent verbal and written communication abilities - Proficiency in Microsoft Office tools - Attention to detail and ability to work independently Please note that the company provides health insurance as a benefit and the work location is in person with a day shift schedule.,