Statistical Programmer - job 1 of 3

Job Summary

A company is looking for a Statistical Programmer.

Key Responsibilities

• Provide programming support for Phase 1 to Phase 3 studies, including project integration and disease monitoring
• Create and review annotated CRF to SDTM datasets and ensure timely project deliverables
• Collaborate with various departments to enhance communication and promote process improvements

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, including SDTM, ADaM, and controlled terminologies
• Strong organizational skills with the ability to prioritize tasks effectively