Job Details

A company is looking for a Statistical Programmer to provide programming expertise for clinical studies and regulatory submissions.Key ResponsibilitiesLead statistical programming activities to ensure timely and high-quality deliverablesDevelop and maintain programming documentation and create CDISC standard specificationsSupport global regulatory submissions and mentor junior programmersRequired QualificationsMinimum Bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science or related discipline2-12+ years of programming experience in processing clinical trial dataProficiency in SAS programming; knowledge of R or Python is a plusExcellent knowledge of CDISC standards and regulatory submissionsHands-on programming and people management experience