November 1
• Perform the role of the Lead Statistical Programmer • Plan, execute and oversee all programming activities on a study • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs • Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated CRFs and Reviewers Guides • Develop specifications for SDTMs and ADaM datasets • Review SAPs and TFL shells from a programming perspective for studies • Mentor less-experienced programmers in the processes around SDTMs, ADaMs and TFLs • Present and share knowledge at department meetings • Respond to QA and client audits, and support qualification audits • Identify processes within programming that will increase productivity, quality and efficiency
• 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 • Typically, 3-5 years of SAS® programming experience in the CRO or Pharmaceutical industry, or an equivalent combination of education and experience • Knowledge of CDISC requirements • Needs Oncology lead experience • Typically, 3-5 years of Oncology experience • Submissions experience is preferred
• Comprehensive benefits including: Medical, Dental, Vision, Life, STD/LTD, 401(K), ESPP, Paid time off (PTO) or Flexible time off (FTO), Company bonus where applicable.
Apply NowNovember 1
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