BSc in Computer Science, Mathematics, Statistics or related area with relevant experience
At least 7 years of experience in either clinical programming and/or statistical programming, within the CRO/pharmaceutical environment using SAS Software
In depth understanding of clinical programming and/or statistical programming processes and standards
Extensive experience with statistical programming using the SAS software including development and use of SAS Macros. Strong programming and problem-solving skills
Trained / hands on experience of R Programming
Advanced knowledge in CDISC standards (CDASH, SDTM, ADaM)
Proven experience in leading programming activities for pooled and exploratory analyses across multiple clinical studies and submission activities (or equivalent)
Proven ability to work effectively both independently or in a team setting, and to meet set goals by managing own timelines
Experience working in cross-functional, multicultural and international clinical trial teams
GK
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