Job Summary
A company is looking for a Senior Statistical Programmer responsible for providing statistical programming services for assigned clinical trials.
Key Responsibilities
- Act as the lead programmer for complex clinical trials and coordinate activities for support programmers
- Design, develop, document, and validate tools and macros to enhance quality and efficiency
- Train and mentor team members while participating in business development and SOP development
Required Qualifications
- Degree in Statistics, Computer Science, or a closely related field; work experience may substitute for degree
- Minimum of 6 years of direct SAS programming experience in pharmaceutical development or CRO environment
- Good knowledge of medical terminology and clinical trial analysis
- Familiarity with relevant industry data standards such as CDISC SDTM and ADaM