Clinical Trial Assistant

Job Summary

Supporting the SELUTION SLR clinical program, the full-time remote Clinical Trial Assistant will manage invoicing duties, assist with study site coordination, and maintain Trial Master Files while ensuring compliance with industry regulations.

Key responsibilities

• Assist in the invoicing process and facilitate communication between clinical vendors and accounts payable
• Support study site activities to ensure adherence to study protocols and regulatory compliance
• Maintain internal Trial Master Files and prepare documentation for audit readiness

Required qualifications

• Minimum of 1 year of experience in clinical studies with knowledge of ICH and GCP guidelines
• Bachelor's degree or equivalent education
• Experience in the medical device or regulated manufacturing industry is preferred
• Proficiency in Microsoft and other computer software packages
• Strong communication skills and ability to work both independently and in a team environment