The Principal Clinical Contract Analyst supports global clinical research by leading the development, negotiation, and execution of complex clinical trial agreements, budgets, and related site documents. The role partners with clinical operations, legal, finance, and study teams to help ensure studies are initiated efficiently and conducted in compliance with applicable regulations and organizational standards. The work contributes to the development of medical devices and digital health solutions for people living with diabetes. The analyst administers standard and nonstandard contracts, conducts proposal preparation and contract negotiation and administration, and supports contract acquisition and fulfillment in accordance with company policies, legal requirements, and customer specifications. The role examines cost estimates, performance requirements, and delivery schedules; prepares bids and reports; advises management on contractual rights and obligations; and maintains historical data. The position operates with considerable latitude and limited managerial oversight, coaches and delegates to lower-level specialists, and contributes to business-strategy-based direction for products, processes, standards, and operational plans. It may manage projects or processes extending beyond the immediate job area and independently develop solutions or improvements to moderately complex problems. The analyst communicates with internal and external customers and vendors at various levels.
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Job Type
Full-time
Career Level
Principal
Education Level
High school or GED