I have more than 16 years of thorough experience in the Clinical (SAS®) Programming area for the Pharmaceutical Industry into roles demanding
hands-on programming, oversight and project management, defining specifications, ensuring data quality, scheduling work and resource levels, deliverables
and regular liaison between customers and study teams.
Having previously worked in Clinical Research Organisations (CROs) in roles of increasing responsibility including Senior Programmer,
Project Manager and Head of Department, I understand the importance of meeting your timelines in a cost effective way while maintaining
quality. I have a sound understanding of International Conference on Harmonization (ICH), Good Clinical Practice (GCP), CDISC SDTM, CDISC
ADaM and am an active member of ISCR and PhUSE.
I am passionate about exploring new and innovative ways of problem solving.
Specialties
- Statistical Reporting and Mapping using SAS, CDISC SDTM and ADaM
- PK/PD NONMEM ready derived dataset generation
- Setting up data and programming standards
- Process Automation, Continuous Improvement (Kaizen), Six-Sigma Green Belt champion
- Application Development to build efficiencies in processes
- SAS Base 8 Certified with strong SAS Macros/SQL skills
- Smart electronic data capture techniques using Adobe Livecycle Designer ES2
- Web technology with hands-on knowledge: HTML, XML, ASP.NET, JS, CSS, PHP, web-based JS Charts
