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Job Description:
Description
Develop, maintain, and validate SAS programs under the direction of senior programming or biostatistics staff
With support from senior programming staff, develop specifications for datasets or TLFs as needed
Execute all programming activities on a study, including but not limited to, resource estimation, working within budget, meeting timelines, maximizing efficiency, etc.
Interact and effectively communicate with members of programming and biostatistics department, other departments (such as clinical data management, medical writing, clinical operations), and the client
Continually identify and suggest ways to improve the efficiency, quality and productivity of statistical programming
Education/Qualifications
Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects.
Experience and/or education plus relevant work experience, equating to a Bachelor's degree
Experience
1-2 years of SAS® programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience
Knowledge of CDISC requirements preferred
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