Biostatistician
Current• Managing clinical research activities• Management of clinical coordinators and research nurses• SAS (Statistical Analysis System) programmer• Grant writing• Statistical consulting for anesthesia and orthopedics departments on all aspects of experimental studies, from study design to analysis and write-up. Provide broad statistical support, including trial design, protocol and CRF development• Develop statistical methods sections of protocols, articles and project reports• Perform sample-size calculations, generate randomization lists and write statistical methodology sections for inclusion in study protocols• Provided data cleaning, data manipulation, and survey data scoring, to provide descriptive and analytic reports, and to perform exploratory and specialized statistical analyses such as missing data imputation. • Protocol development, sample size calculation, construction of protocols and CRFs• Survey construction, item evaluation and analysis• Created and submit documents (all aspects: consent forms, protocol, CRFs, etc..) to IRB.• Case report form (CRFs) construction and associated data entry sheets in Excel, MS Access, SAS and CSV files for import into SAS (or SPPS, R, S+, Matlab, etc.). • Data management• Database design• Variable selections and quantification, • Validation checks.• Data consistency checks and data validation, • such as data entry cross checking and analysis of missing data patterns.• Create presentation quality tables and figures for manuscripts.• Coordinate with multi-center studies re: study protocol or statistical analysis. • Interpret analyses and write statistical sections of study reports.• Developed and taught internal and external statistical training seminars, lectures and courses.• Present posters and give lectures at anesthesiology meetings.• Manage study team members with regards to study execution as it relates to timelines, data quality, and interpretation of results.
