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Position: Statistical Programmer
Duties: Responsible for the integrity of the programming/computing solutions for multiple clinical trials (or equivalent) and/or publication activities; In collaboration with with the Biostatistician and Senior Programmer, provide programming support to project-level programming deliverables and other ad hoc programming requests; Ensure understanding and compliance with study and project programming standards. Responsible for development of programming specification; Support the full execution of final production run and programming activities for a project or an indication with guidance from senior team members; Maintain optimum communication with internal and external study team members, Lead Programmer and Lead Statistician and provide status of programming activities as and when required. Maintain up-to-date, accurate progress of the assigned programming deliverables and ensure high efficiency and timely completion according to agreed timelines, report to Lead Programmer and/or Lead Statistician in case of any potential challenges
Requirements: Graduates/Post Graduates or equivalent experience in mathematics, statistics, computer science, health sciences or related fields; At least 2 years of work experience in a programming role preferably supporting clinical trials/or in the pharmaceutical industry (1 year experience for MS Statistics/Computer Science graduates).Intermediate understanding of global clinical trial practices, procedures, methodologies; Good knowledge of/experience with SAS (including SAS/Base, SAS/Graph and SAS/Macro) and other relevant programming software. Solid understanding of office tools (mainly Excel, Word) and database design/structures and basic statistics; Intermediate in Mandarin Language
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