Develop SAS programs for SDTM, ADaM, client-defined analysis datasets, Patient
Profiles, Tables, Listings and Graphs in support of the Statistical Analysis Plan, posters,
manuscripts, Integrated of Summary of Safety (ISS) and Integrated Summary of
Provide technical planning to include overseeing the set-up of key macros and SAS
Act as a Lead Programmer for projects
Represent Statistical Programming at internal and client meetings
Act as a Statistical Programming consultant to clients and internal customers in related
disciplines e.g. Clinical Data Management, Project Management and Medical Writing.
Demonstrate excellent problem solving skills, a proactive approach and a willingness to
make decisions on a regular basis.
Ensure quality of personal work and the work of the team when acting as a Lead
Prioritize personal workload and that of teammates; perform work with minimal
Work on complex problems where analysis of situations or data requires an evaluation of
intangible variables; development of technical solutions to abstract problems which
require the use of ingenuity and creativity.
More than 4 years experience with proven SAS skills within a clinical trials environment.
Knowledge in all aspects of clinical trials from initial study set-up to study completion.
Full knowledge and understanding of the processes and procedures used within a
Statistical Programming environment.
Able to identify training and development needs, opportunities for optimizing staff
utilization and employing the most efficient practices.
Excellent organizational skills and the ability to delegate and prioritize work to meet tight
deadlines while maintaining high standards
Self motivation and ability to work independently with minimum direction.
Sorry the Share function is not working properly at this moment. Please refresh the page and try again later.
Share on your newsfeed