Clinical Statistical (SAS) Programmer

Responsibilities for Clinical Statistical (SAS) Programmer: Generate datasets, tables, listings, and figure outputs per project requirements utilizing SAS programming. Actively communicate with clients to update on progress of projects. Review and revise code, programs, and technical documentation. Assist in establishing standardized programming procedures and work instructions. Technical Requirements for Clinical Statistical (SAS) Programmer: Minimum 5 years of experience with SAS programming with clinical trial data Strong background working in a CRO or Pharmaceutical environment Bachelor's or Master's degree in Statistics, Computer Science, or related field Expert knowledge in CDISC implementation guidelines (SDTM / ADaM)