Associate Director Statistical Programming
A company is looking for an Associate Director, Evidence Generation Statistical Programming. Key Responsibilities Provide statistical programming support for regulatory submissions and ensure compliance with CDISC standards Develop programming standards and templates to enhance efficiency and quality in clinical trial data analysis Evaluate and improve the computing environment system for programming and analysis efficiency Required Qualifications Bachelor's Degree in a science or technical field; Master's Degree preferred 10+ years of experience in the pharmaceutical industry or CROs with a Bachelor's degree; 7+ years with a Master's degree Experience in SAS macro and/or system utility development preferred Advanced knowledge of SAS programming and CDISC SDTM/ADaM implementation Understanding of statistical concepts and drug development phases preferred
