Leading statistical activities for clinical trials, the full-time Senior Statistical Programmer will program and validate datasets, oversee programming deliverables, and collaborate with cross-functional teams in a remote environment. Key responsibilities Program and validate derived datasets, tables, figures, and listings for clinical trials Ensure timely and high-quality programming deliverables while managing internal contractors and external vendors Participate in the development of departmental working instructions and guidelines Required qualifications Bachelor's or Master's degree in Computer Science, Mathematics, Engineering, Medical, or related discipline More than 5 years of experience with a BS or 3 years with an MS in statistical programming (SAS, R) in the pharmaceutical industry Strong knowledge of SAS and SAS Macro language, as well as R programming skills in clinical trials Familiarity with the drug development process and industry standards Ability to work on data integrations (ISS and ISE)
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