Andrew Powers is a clinical research and R&D systems professional based in Media, Pennsylvania, serving the Greater Philadelphia life-sciences community and working with distributed clinical-development teams.
His experience spans TMF/eTMF operations, Veeva Vault Clinical Operations applications, regulatory submissions, clinical compliance, business and systems analysis, operational reporting and process improvement.
Andrew has supported cross-functional study teams by translating operational needs into system requirements, dashboards, metrics, workflows, change requests, testing and validated system enhancements. His TMF work includes health reporting, completeness, timeliness and quality oversight, vendor governance, inspection readiness and the use of operational data to identify risk and drive corrective action.
Professional approach
Andrew's work emphasizes practical, measurable improvements: defining the business problem, establishing meaningful metrics, identifying root causes, aligning stakeholders on actions and measuring whether the change improved performance.
Core subject areas
Trial Master File operations; eTMF; Veeva Vault; clinical operations; R&D systems; TMF reporting and dashboards; inspection readiness; vendor oversight; requirements; UAT; validation; data migration; and process improvement.