I am a senior certified SAS consultant.
I specialize in producing research data marts, publication-ready reports and analysis for scientific researchers.
My background includes:
- Base SAS Software
- SAS Macro Facility
- SAS/AF and web applications
- SAS Component Language
- SAS/STAT
- SAS/Graph
- ODS Reporting
- I have taken over 20 SAS courses from SAS Institute.
- I have been certified in every version of SAS software from V6.12 to V9.
- I have been a member of the SAS Partner Program since its inception in 1997.
- I attend global, regional, and local SAS conferences every year, sometimes as a presenter.
- Phase I-IV clinical trials in the U.S. and Europe. Therapeutic experience in oncology, infectious diseases.
- Health care claims analysis: medical, inpatient, outpatient and pharmacy.
- Complex multi-year, multi-national high-profile disease management programs.
- CDISC standards.
- Clinical data coding standards such as MedDRA, WHO-Drug, ICD-9 diagnosis codes, CPT procedure codes.
- Sole authorship of complete clinical study reports.
- Attendance at meetings between FDA advisory committees and sponsors.
- SAS programming for NDA submissions, annual reports, safety summaries and other regulatory submissions.
- Clinical data management, site monitoring and medical writing.
- Authorship of SOPs.
- Attend DIA conferences.
- Microsoft Windows, including Windows 7
- UNIX
- JavaScript
- Web analytics using Google Analytics and SAS
- Technical writing
- Demonstrated commitment to learning new technologies and to teaching others.
