Description
Statistical Programmer* Review protocols, statistical analysis plans and case report forms, and provide SAS data specifications for clinical trials
* Ensure programming deliverables are consistent and comply with study protocols, statistical analysis plans and case report forms
* Work under the supervision of project statistician to coordinate with data management and clinical operation to ensure quality of clinical trial databases
* Develop standard programs to facilitate general programming requirement in clinical trials
* Provide ad-hoc analysis programming to explore repository databases and to support publications
* Ensure implementation of corporate standardized programming conventions and working guidance
CANDIDATE'S PROFILE
Education / Professional experience
* Master's or equivalent degree in Biostatistics, Statistics, Epidemiology, Mathematics, Computer Science, Life Sciences or related field
* 5+ years of pharmaceutical experience
* Excellent knowledge of CDISC-compliant SAS data structures and other related regulatory guidance
To find out more about Real please visit www.realstaffing.com