A company is looking for a Senior Statistical Programmer, proficient in R, for a permanent role.
Key Responsibilities
Program and validate 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 standards and guidelines
Required Qualifications
Bachelor or Master degree in Computer Science, Mathematics, Engineering, Medical or related discipline
5+ years of experience with a BS or 3+ years with an MS in statistical programming (SAS, R) in the pharmaceutical industry
Working knowledge of SAS and R programming in clinical trials
Familiarity with the drug development process and industry standards
Ability to work on data integrations (ISS and ISE)
Senior Statistical Programmer • Raleigh, North Carolina, United States
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