Job Summary
A company is looking for a Statistical Programmer Consultant to provide programming support for Phase 1 to Phase 3 studies.
Key Responsibilities
- Involved in programming activities across multiple projects/studies in various therapeutic areas
- Creates and reviews annotated CRF to SDTM datasets and provides support for project deliverables
- Collaborates with various departments to meet timelines for statistical data analysis and reporting
Required Qualifications
- Master's Degree in Statistics, Computer Science, Mathematics, Engineering, or related discipline
- 1-5 years of clinical trial programming experience in the biotechnology or pharmaceutical industry
- Advanced SAS programming skills and experience with statistical software such as R and S-Plus
- In-depth knowledge of CDISC standards including SDTM and ADaM
- Self-directed with strong organizational skills and ability to prioritize tasks
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