Created tools in the form of reports and interactive dashboards for primary care providers, pharmacists, and C-level executives for monitoring the effectiveness of value-based cared initiatives at an accountable care organization. Data was aggregated from medical claims, pharmacy claims, and electronic medical records.- Designed Tableau dashboards that displayed key clinical metrics, such as clinical readmissions rates by discharge unit, and HEDIS metrics required for value based care.- Collaborated with pharmacy managers to provide custom data analytics using Python and R. This included calculating potential cost-savings from switching a percentage of our attributed population from proprietary medications to generics- Created data pipelines that moved data from raw text files to relational databases.

Produced high-quality laboratory safety and microbiology datasets in support of clinical trials by performing data management activities using SAS 9.4. Worked with external clinical data managers at contract research organizations to define the structure and content of datasets and resolve data reconciliation issues.- Standardized extraction of clinical data from a clinical database by writing SAS macros . - Wrote programs using SAS to create datasets that complied with CDISC study data tabulation models (SDTM), and mapped clinical laboratory results according to CDISC SDTM controlled terminology.- Wrote SAS macros to automatically calculate toxicity grading for laboratory safety results as outlined in CDISC SDTM implementation guide version 3.2 for the laboratory safety (LB) CDISC domain.

Authored data transfer agreements between ACM Global Laboratories and clinical research organizations and ensured that laboratory safety data transfers adhered to the structure and format defined in this document. Acted as an internal resource for data analytics projects that addressed operational and scientific questions.- Created a script using R that aggregated the data of approximately 2000 separate Excel spreadsheets, performed data validation and cleaning, and summarized the data across all files.- Created interactive data visualizations of clinical trial performance metrics using R/RShiny and static metrics reports using R/rmarkdown. The data visualizations and reports retrieved data from an SQL database and displayed common quality issues made by clinical trial investigator sites across entire studies, with a breakdown of which errors were most prominent at each investigator site.- Assisted Scientific Affairs department in various requests for organizational analytics. Deliverables included statistical analysis of data generated by laboratories in the United States, United Kingdom, and Singapore.

Supports the day-to-day activities of an academic research laboratory by maintaining a MySQL database of lab results, performs data analysis using R and Python, and works closely with the Upstate Stem Cell cGMP Facility to produce cGMP grade material for pre-clinical animal efficacy studies.

Specialized in testing the removal of viruses from biological samples by column chromatography, filtration, and solvent treatments in a GLP regulated laboratory environment. Testing supported data packages for outside pharmaceutical companies and medical device manufacturers to show compliance with FDA Q5A Viral Safety Evaluation of Biotechnology Products Derived From Cell Lines of Human or Animal Origin

Produced investigative vaccines against various strains of Escherichia coli, which involvedperforming fermentation of recombinant E. coli and using the resulting biomass as startingmaterial for column chromatography.