Clinical Trial Assistant

Job Summary

To support the start-up and ongoing coordination of clinical research sites, the part-time Clinical Trial Assistant will manage site activation milestones, regulatory document management, and serve as a communication point among stakeholders in a fully remote contract role.

Key responsibilities:

• Support site feasibility assessments and assist with site selection and study start-up documentation
• Request, review, and track essential regulatory documents to ensure compliance with GCP and regulatory requirements
• Coordinate study meetings and communications, and assist with Site Initiation Visit preparation

Required qualifications:

• Bachelor's degree in Life Sciences, Healthcare, Nursing, Public Health, or a related field
• Relevant experience in clinical research, clinical trials, or site management
• Proficiency with Microsoft Office Suite and experience with clinical research technologies
• Working knowledge of Good Clinical Practice (GCP) and clinical trial regulations
• Strong organizational skills and ability to manage multiple priorities effectively