What You'll Do:

• Uses logistics experience to plan, document, and facilitate global cross-border supply strategies, including compliance to global trade standards, and in-country permitting requirements to facilitate delivery of products (e.g., clinical specimens, supplies, research materials etc) to final destinations
• Attends clinical project meetings for relevant information and translate clinical trial protocol information into supply plans, which meet critical timeline and budget targets
• Provides risk-mitigation strategies to avoid undue delays or expenses with the supply chain
• Tracks and prepares shipment journey information utilizing databases, spreadsheets, and other tools to ensure material stability and on time requirements
• Builds business relationships with couriers and establishes a working knowledge of using the appropriate logistics software and databases
• Ensures shipping materials are appropriately validated per regulatory requirement

What You'll Bring:

• Knowledge of biological tissue transportation and logistics
• Ability to work well in a rapid-pace startup environment
• Excellent verbal and written communication
• Proficient with Microsoft Word, PowerPoint, and Excel
• Self-starter, possessing a strong work ethic, ability to drive change, and passion for helping others
• Minimum of 1 year of central lab and/or clinical research experience or possesses transferable skills

About CTI

CTI Clinical Trial and Consulting Services is a global, privately held, full-service clinical contract research organization (CRO) focused on the advancement of treatments for chronically and critically ill patient populations. We assist clinical research throughout the lifecycle of development, from drug concept to commercialization. CTI is headquartered in the Greater Cincinnati, OH region with global operations in collaboration with pharmaceutical, biotechnology, and medical device firms. For more information, visit www.ctifacts.com