Clinical Trial Assistant

📋 Description

• Coordinate and manage the ordering, shipping, labeling and tracking of study supplies (including
• Establish, organize and maintain trial master file and clinical trial management system to ensure
• Contribute to operational excellence and continuous improvement
• Maintain, track and facilitate routing for approval and signature of clinical study documents
• Create purchase requests and process invoices
• Support clinical study manager with study budget tracking and payments of clinical sites and vendors

🎯 Requirements

• Excellent communication, organization and interpersonal skills with strong attention to detail
• Strong ability to organize, prioritize and manage multiple priorities
• Prior experience in medical device clinical trials, regulatory support, clinical project
• Proficient in MS Office suite, Adobe, video and web conferencing solutions
• Clinically savvy & good knowledge of basic medical terminology preferred
• Possess working knowledge of Good Clinical Practice as detailed in 21CFR and ISO 14155, and

🎁 Benefits

• Market-competitive compensation packages, inclusive of base pay, incentives, benefits and equity