Biostatistician
Resume:
Ben Wang
actk6j@r.postjobfree.com
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: L inear 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: C linical Trial Phases and Design
PROFESSIONAL EXPERIENCE
Roche Molecular
04/2014 – Current
Biostatistician
Responsibilities:
● Therapeutic areas: HPV, HIV, HBV, HCV, CMV, Lung Cancer
● Research new methodology: Passing Bablok
● Create and present macro implementing method
● FDA submission of Clinical Study Reports
● Addressing FDA requests
● Statistical Analysis Plan creation
● Study Design
● Protocol development and review
● Case Report Form review
● Ad hoc Requests
● Design of tables, listings, figures
● Randomization
● Analysis Data Specs creation
● Guide programmers to create Tables, Listings, Figures Novo Nordisk
06/2013 – 4/2014
Biostatistician & Statistical Programmer
Responsibilities:
● Therapeutic areas: diabetes (inflammation, growth hormone)
● Clinical Study Report, Protocol, and Case Report Form review
● SAP editing
● CDISC analysis data specification review and QC
● SAS Macro development for graphical displays, tables, listings
● Creation of Tables, Listings, Figures
● 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
● Conduct 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.
● SAS and Excel were used for data managing
● Obtained preliminary results and presented findings
● Provide statistical reviews of proposed design and analysis of protocols for investigator initiated trials.
● Provide statistical input for design, sample size, protocol, and CRF for studies.
● Provide review of statistical analysis plan (SAP) including table shells, analysis dataset specifications and all deliverables for studies provided by CRO
● Manage outside CROs and consultants as needed.
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
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