Procurement Analyst I

Clinical Procurement Consultant We are looking for a Clinical Procurement Consultant to help with a specialized data-cleansing and harmonization project. The goal is to transform unstructured clinical site budget data into a structured format to support Fair Market Value (FMV) benchmarking and financial compliance. The ideal candidate is a self-starter who understands the complexities of clinical trial costs and can independently navigate internal systems to ensure data integrity and audit-readiness. Key Responsibilities Data Harmonization: Review and standardize unstructured data from clinical site budgets, ensuring consistency across diverse global sites and trial phases. FMV Analysis: Align budget line items with Fair Market Value (FMV) standards to ensure compliance with industry regulations and internal financial thresholds. System Integration: Map legacy and unstructured data into internal tracking tools and databases, resolving discrepancies in terminology and categorization. Process Documentation: Develop clear workflows and "Source of Truth" documentation to maintain data quality for future trial budgeting. Stakeholder Collaboration: Work closely with Clinical Operations and Clinical eSolutions teams to validate cost assumptions and procurement benchmarks. Required Experience & Skills Clinical Background: Deep familiarity with clinical trial terminology, Site Payment schedules, and Clinical Trial Agreements (CTAs). Procurement & Finance: Experience in clinical sourcing, cost-benchmarking, or financial analysis within the diagnostics industry. Data Proficiency: Skilled in Excel (Pivot Tables, Data Validation) and comfortable working with internal proprietary software, Tableau. Compliance Mindset: Understanding of the regulatory landscape surrounding investigator payments and financial transparency. Professional Attributes Self-Directed: Able to operate with minimal supervision and define a path forward when faced with ambiguous or "messy" datasets. Detail-Oriented: A "quality-first" approach to data, ensuring every entry is defensible for potential audits. Adaptive: Quick to learn internal tools and adapt existing clinical knowledge to proprietary company workflows. 2-3 years of experience in a similar role. Schedule 7am-7pm (needing flexibility) 8 hr shift Interview process 1. phone or virtual 2. Virtual panel Hybrid Tuesday & Friday anchor days Notes In direct exp or clinical trial budget experience, data clean up, attention to detail, high volume, possible extension #J-18808-Ljbffr