Clinical Trial Assistant

📋 Description

• Coordinate ordering, shipping, labeling and tracking of study supplies
• Maintain trial master file and CTMS for regulatory and protocol compliance
• Support study budgets, payments to sites and vendors
• Prepare and ship site and patient binders as needed
• Create study materials and collaborate with CSM/CRA for study execution
• Schedule and plan meetings, distribute agendas and minutes

🎯 Requirements

• Strong communication, organization and attention to detail
• Ability to manage multiple priorities
• Experience in medical device clinical trials and regulatory support
• Proficient in MS Office, Adobe, video/web conferencing
• Knowledge of GCP (21 CFR) and ISO 14155; 21 CFR Part 812
• 2-4 years clinical research experience; bachelor’s degree preferred

🎁 Benefits

• Market-competitive compensation with base pay and incentives
• Benefits and equity; compensation ranges depend on location/experience