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Senior Statistical Programmer

Laboratory Corporation of America Holdings (Covance)

Shanghai, China

Job Overview: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 Efficacy (ISE) Provide technical planning to include overseeing the set-up of key macros and SAS programs. 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 Programmer Prioritize personal workload and that of teammates; perform work with minimal supervision 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. Education/Qualifications:5 - 8 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. Experience:5 - 8 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.

Job posted: 2020-06-04

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