2+ Years in Statistical Programming: Proficient in dataset manipulation, variables derivation, data visualization, macro programming, and statistical procedures using SAS and R.
Experience in CRO and Hospital: Proficient in phases II-III clinical studies, covering various therapeutic areas including oncology, endocrinology, nephropathy, etc.
CDISC Standards: Experienced in SAS/R programming under CDISC, including SDTM/ADaM in both production and validation side.
Data Visualization: Expert in generating Tables, Figures, Listings and creating customized output files.
Analytical Skills: Strong analytical capabilities in statistical methods and SAS/STAT procedures including PROC MEANS, PROC FREQ, PROC GLM, PROC LIFETEST, PROC PHREG.
Document Review: Experience in CRF annotation, Specification write and review, Statistical Analysis Plan review, and review Pinnacle 21 data conformance report.
Team Collaboration: A proactive team player bringing enthusiasm to group efforts. Communication: Excellent oral and written communication with remarkable problem-solving skills.
Overview
3
3
years of professional experience
2
2
Certifications
6
6
years of post-secondary education
Work History
Statistical Programmer
JN Data Resolution
06.2023 - Current
Performed SAS programming to support Phase II-III clinical trial study including obesity, type II diabetes
Developed and validated SDTM and ADaM datasets for both safety and efficacy
Utilized PROC LIFETEST to perform survival analysis and generated Kaplan-Meier plot using PROC SGPLOT, with the p-value from log-rank, and customized legends
Collaborated with statistician to generate and test efficacy/safety tables and figures to support publication
Produced data conformance reports for SDTM and ADaM XPT datasets by using Pinnacle 21, and gave comments on the Pinnacle 21 report
Complete ad-hoc and urgent requests and from other studies using SAS and R
Participated in project team meetings, programming group meetings for timeline assignment, delivery package, data issues, etc.
Research Analyst
Xijing Hospital
03.2022 - 03.2023
Worked on a cohort study on IgA nephropathy, advancing understanding of tacrolimus’ safety and efficacy
Performed sample size and power calculations, elevating statistical robustness in data analyses
Provide recommendations for optimal statistical analyses and study design to the research team
Ensure the accuracy and timely delivery of summary reports, tables, and figures to the research team
Co-authored a renowned pharmacology publication, showcasing potent interpersonal and collaboration skills.
Education
Master of Science - Biostatistics - Data Science Track
Columbia University
New York, NY
09.2021 - 05.2023
Bachelor of Science - Statistics
University of California, Davis
Davis, CA
09.2017 - 06.2021
Skills
SAS (SAS/BASE, SAS/STAT, SAS Macro)
Certification
SAS Certified Professional: Advanced Programming Using SAS 9.4, 03/2023
Publications
Efficacy and safety of tacrolimus-based treatment for non-rapidly progressive IgA nephropathy, Frontiers in Pharmacology, Vol. 14, 05/2023, 10.3389/fphar.2023.1189608