Responsibilities
The role involves participating in all statistical programming activities, including preparing clinical data for submission using CDISC standards and developing SAS programs for analysis datasets and TFLs. Additionally, the programmer will mentor team members and may manage project timelines, scope, and budgets.
Requirements
Candidates must hold a bachelor’s degree in statistics, computer science, or a life science discipline. A minimum of 8 years of experience in statistical programming within clinical trials is required, along with proficiency in CDISC standards and SAS programming.
