As a WEDI co-chair of Genomics the aim is enhance the exchange of clinical and administrative healthcare information to make a far reaching impact across the industry.

As the Clinical Lead for the InterQual Molecular Diagnostics and Durable Medical Equipment products I support the development of evidence based clinical decision support solutions that help ensure clinically appropriate medical utilization decisions.

• Manages the content development for the InterQual Molecular Diagnostic product including the planning, execution, and tracking of dozens of complex project• Collaborats with Medical Director and Clinical Content Developers to assure clinical content accuracy and appropriateness and maintain consistency across products• Manages integrations between InterQual and DEX Diagnostic Exchange related information• Involved in the assessment of proprietary DEX Z-Code™ identifiers and cataloging the test information used as policy management•Serves as an internal trainer for the Clinical department on Evidence Based Medicine training and application to InterQual development• Identifies opportunities for collaboration that build customer satisfaction• Serves as a resource for new and current employees to support orientation of new staff, skill development, product and industry knowledge transfer, application training, and mastery of content development• Participates in presenting internal trainings on content products•Works alongside account executives to ensure customer satisfaction and serves as a direct clinical resource to customers• Participates in the development of clinical training materials and case studies• Provides Customer Service • Managed multiple process improvement projects aimed at developing and documenting new processes, developing policies for existing processes, and streamlining team workflow and organization• Responsible for driving development and execution of clinical content scope to meet financial and operational targets• Extensive use of Sharepoint, MindManager, JIRA, EndNote as well as the Microsoft suite of products including OneNote and familiar with Kanban and Agile development tracking tools

Specializing in clinical criteria associated with the preauthorization of Molecular Diagnostic tests, Specialty Pharmacy treatments and Durable Medical Equipment. Trained in Evidence Based Medicine (EBM) and in coding associated with molecular testing.

As a member of the Advanced Diagnostics Management (ADM) team I help to develop the clinical content and criteria for molecular and genetic tests. The molecular diagnostics (MDx) we develop give physicians and clinical labs intelligent, automated decision support tools at the point of decision that enable transparent, immediate access to coverage, network and utilization rules. The result: better control of MDx medical spending.

Post-doctoral research focusing on the following: cell cycle regulation in mammary epithelial cells, endogenous ligands for the Aryl Hydrocarbon Receptor and CYP450 regulation of growth.

Commencement Speaker (medical and doctoral student graduation)Founding Member, Boston University Graduate Medical Sciences Student OrganizationMedical School Executive and Steering Committee Student RepresentativeAs a PhD candidate I studied the endogenous role of the Aryl hydrocarbon receptor (AhR) in mammary tumor development and the regulation of cell cycle associated proteins (Chk2/p21) by the AhR.