Oversee the modernization effort for data warehousing, analytics, and reporting technologies. Manage mission critical timelines, pipelines, and tasks for the enterprise reporting team. Serve as the liaison between cross-functional business stakeholders and technical team members to deliver data and analytics that align with the business objectives and mission.

Led the implementation of an Enterprise Data Warehouse using Informatica, BigQuery, and Tableau. Led the creation and execution of the Analytics Center of Excellence by developing a team of data professionals. Served as the Lead of the Data Governance Council.

Serve as a stakeholder, project manager, and developer for data products in a newly established Looker platform including specifications, LookML development, dashboard design and implementation, and query optimization to convey key performance indicators, outcomes, and trends in medical practice across a number of cardiac procedures.Lead a dedicated team of developers and quality assurance experts to work with internal stakeholders and external clients to define and implement clinical trials, generate specifications, deliver high quality aggregate reports, and determine roadmaps and processes.

Integrate patient and parent reported data with clinician and investigator entered data through the use of Global Unique Identifiers. Perform clinical and genomic data analysis and generate static and interactive reports for internal use, end users, the Advisory Committee on Heritable Disorders in Newborns and Children, presentations, and publications. Perform website, tools, and business analytics and generate reports. Perform impact assessments of tools, training plans, and implementation efforts.Aid the Project Director in tracking, generating, and submitting all contract deliverables for the Eunice Kennedy Shriver National Institute of Child Health and Human Development (NICHD). Generate and provide written functional and technical requirements and milestones. Track and maintain the budget for the Coordinating Center and subcontractors including monthly reports.Generate a training plan for investigators for database and tool use, including an annual workshop, quarterly webinars, instruction videos, and case studies demonstrating the utility and applicability of various post-analytic tools. Aid in writing and information technology (IT) plan which meets the National Institutes of Health (NIH) FISMA Moderate Security Requirements.

Planned and implemented new longitudinal clinical studies and maintained existing studies using REDCap and other tools in the Longitudinal Pediatric Data Resource (LPDR). Worked with researchers to define common data elements (CDEs), data collection plans, and analysis plans. Provided data analysis in Tableau at regular intervals for clinical data, project management data, and ACMG Foundation data.Served as the Application Steward for (1) 3 REDCap instances; including software upgrades, code changes, helpdesk support, user and permissions tracking, and project tracking as part of the Privacy Impact Assessments, and (2) Confluence and JIRA; including maintaining software compliance through upgrades and scanning, generating workflows and spaces, and tracking and implementing users and permission schemes.Developed and maintained deliverables timelines and monitoring for all security documentation and submissions. Generated and performed yearly reviews of security and system documentation to maintain the Authority to Operate. Acted as a member of the Enterprise Security Team and FISMA Control Board.

Implemented electronic case report forms for new studies using REDCap and other tools. Worked with clinicians and researchers to define CDEs and data collection plans. Generated comparisons for standardization efforts across the project including analysis in Excel and Tableau.Worked with the ACMG Security Team to aid in system documentation and appropriate FISMA and project deliverables including the Implementation of annual security awareness training for all ACMG staff.

-Coordinate all aspects of Data Management for the Clinical Trials product line. This includes management of CRF and data transfer development in accordance with GCPs and SOPs, maintaining code, and working with project managers and IT to identify and implement solutions to customer requests.-Lead and coordinate all aspects of Data Management for the Registries product line. This includes managing data mapping for data integration projects, developing forms, and developing special projects.-Deliver data to customers including pulling data from the database, performing quality checks on the data, coordinating the cleaning of the data, and meeting deadlines for delivering high quality data.-Maintain, develop, and test code including data transfer scripts, adverse event reports, and electronic forms such as CRFs.

-Coordinated the project team for a collaboration with the Newborn Screening Translational Research Network and national grantees to define datasets for 46 newborn screening disorders under a contract to the American College of Medical Genetics and Genomics-Led development of the Longitudinal Pediatric Data Resource, a combined system of electronic data capture in REDCap, centralized data management, unified data representation, and case reporting within a FISMA-compliant architecture-Developed and implemented educational and training materials-Composed and assessed scientific publications and presentations related to project components-Prepared materials for grants, contracts, and budgets associated with the project-Created and maintained project timelines and assigned duties as necessary

-Worked with clinicians and researchers in the Cardiac Center to develop tools to integrate clinical data from multiple clinical databases-Created CardioDD, an online dictionary tool to standardize definitions and data across echocardiogram protocols