1. Ben Wang
ben.wang8844@gmail.com
908-399-2503
US Citizen
PROFESSIONAL SUMMARY
Experienced Biostatistician knowledgeable in study design, data analysis, and clinical trails. Works well
on a team being flexible and an effective communicator. Hands-on experience with statistical software
packages such as SAS, R, and S-plus, adhoc requests, protocol development, randomization, statistical
analysis plan implementation, designing mock tables/listings/figures, statistical analysis report / clinical
study report writing,researching new methodology and implementation.
SKILLS OVERVIEW
● Statistics/Biostatistics: Linear and nonlinear models, Survival analysis, Dose response,
Pharmacokinetics/pharmacodynamics, Reproducibility, Deming regression (Passing Bablok),
Sensitivity/specificity
● Languages: SAS, R and S-plus
● Software: SAS/Base, Stat, SQL, Macro, Graph, Report, MS Office Suite.
● Therapeutic Areas: HPV, HIV, HBV, HCV, CMV, Oncology Phase III, Diabetes Phase II and III,
Hemophilia Phase III, Cardiovascular Phase III
● Training: Clinical Trial Phases and Design
PROFESSIONAL EXPERIENCE
Roche
04/2014 – Current
Biostatistician
Responsibilities:
● Therapeutic areas: HPV, HIV, HBV, HCV, CMV, Lung Cancer
● New macro implemented and presented to Biometrics department-
o Deming regression confidence bands
o FDA request for Passing Bablock regression
● FDA submissions of Clinical Study Reports: HPV, HIV, Lung Cancer
o Addressed FDA requests- verification bias adjustment with bootstrapping
o Connected with Data management and CRA departments
▪ Data monitoring reports/ patient tracking
o Case Report Form Review
o Analysis Data Specifications
o Statistical Analysis Plan creation
▪ Managed SAS programming team
▪ Created Mock Tables/ Listings
▪ Wrote and implemented Statistical Methods
▪ Produced Statistical Results
▪ Validated Results using SAS
▪ Completed Patient disposition table/ flow chart
● Ad hoc Requests: HPV
o Evaluable patient population with and without vaccination
o By disease endpoint
● Randomization of subjects: HBV, HCV
o Implemented block design by study site
Novo Nordisk

2. 06/2013 – 4/2014
Biostatistician & Statistical Programmer
Responsibilities:
● Therapeutic areas: diabetes (inflammation, growth hormone)
● Reviewed Clinical Study Reports, Protocols, and Case Report Forms
● Edited SAP
● CDISC analysis data specification review and QC
● Developed SAS Macro for graphical displays, tables, listings
● Created of Tables, Listings, Figures for Statistical Report
● QC and Validation including parallel programming, logic checks, proc compare
Bayer Healthcare Pharmaceuticals
05/2012 – 06/2013
Biostatistician & Statistical Programmer
Responsibilities:
● Therapeutic areas: hemophilia, oncology
● Developed Research hypothesis
● Conducted literature reviews and other supporting research
● Assist in clinical study report development (protocol and SAP design, mock tables)
● Assist in data analysis of summary statistics, demographics, statistical modeling, creation of
graphical displays, etc.
● Learned SAS and Excel skills for data managing
● Obtained preliminary results and presented findings
● Provided statistical reviews of proposed design and analysis of protocols for investigator initiated
trials.
● Provided statistical input for design, sample size, protocol, and CRF for studies.
● Provided review of statistical analysis plan (SAP) including table shells, analysis dataset
specifications and all deliverables for studies provided by CRO
Additional experience at Covance 10/2011 - 04/2012
EDUCATION
● MPH in Epidemiology, Rutgers Biomedical and Health Science 2013
● BS in Statistics, Carnegie Mellon University 2011
PRESENTATION
Passing-Bablok Regression A Non-Parametric Procedure for Comparing Analytical Methods
For Roche Biometrics Department 10/2014