Al Turay

Senior Clinical Programming Analyst @Edwards Lifesciences

Irvine, CA, US

Lead the development of highly complex clinical databases, and tools and programs for data validation checks, and clinical trial reporting using SAS, Python and eBuilder Reporter. • Act as a SME on core business software solutions (e.g, Axiom Fusion, RAVE, EDC system and CTMS) to provide novel end-to-end software solutions that improve, automate, and solve complex business process challenges in Clinical Trial Studies.• Plan and lead the design and implementation of complex functional modules and provide clinical programming expertise regarding clinical trials, protocols, and case report form with cross functional teams• Lead the development of specifications for complex systems and/or processes, system upgrades/enhancements and integration; and engage IT to deliver higher level support to users • Plan, organize, and manage internal and external clinical systems resources and activities to support clinical trials in accordance with regulatory and company guidelines. Direct the specification, documentation, validation, implementation, data archiving and retirement activities of clinical databases for clinical studies. • Collaborate with cross functional and other Business Units team to provide functional support to clinical study projects.