Job Description
Major Bio requires SAS Programmer urgently. You must be able to start by 16th/23rd or 30th May at the very latest.
Role is to Provide programming support and validation of analysis data sets, pooled datasets, statistical summary tables, figures and patient data listings for phase I - phase III clinical trials, ISS & ISE, primarily using SAS.
- Provide output for the Clinical Study Report, the Integrated Summary of Safety (ISS), the Integrated Summary of Efficacy (ISE) and electronic submissions.
will work with biostatisticians and programmers based also in other sites - Apply knowledge of clinical data, the design and phases of clinical trials, statistics, relevant regulations and the pharmaceutical industry to the implementation of tasks.
Qualifications/Skills Required
N/A
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