•Manage a team of data configuration programmers •Hire new team members •Strong understanding of clinical research processes including study design, database design, data analysis, and clinical site support •Support multi-site, multi-national infectious disease studies including HIV, STI, ARI, and trauma infectious•Work closely with investigators, project coordinators, biostatisticians, and programmers to develop solutions for individual projects and across the program•Manage many projects simultaneously, evaluate project priorities, and communicate priorities to programming and science teams•Assess budgets, provide cost estimates, and track project status•Coordinate and standardize processes across Data Configuration, Data Management, SAS Programming, and Clinical Research Management teams by developing, documenting, and training on new policies and procedures•Provide high level support for all CDMS users including clinicians, investigators, and analysts

•Participated in medical research study start-up and protocol management•Designed clinical research forms, determined data quality requirements, and wrote logic check standards for data clarification programs•Created and maintained data management plans and standard operating procedures •Wrote training materials and trained data mangers, clinical research coordinators, investigators, and monitors •Interacted with clinical personnel to resolve omissions, discrepancies and other data management issues.•Adhered to a policy of strict confidentiality while maintaining a named subject registry

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