Senior Statistical Programmer
Job Summary
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)
Complete Job Description
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