Leading statistical programming activities, the full-time Manager, Statistical Programming will provide programming expertise for clinical studies, ensuring timely and high-quality deliverables while working in a remote/hybrid environment. Key responsibilities Oversee statistical programming for multiple studies, ensuring adherence to project strategies and high-quality outputs Develop and maintain programming documentation, including CDISC standard SDTM and ADaM specifications Support global regulatory submissions and collaborate with internal and external stakeholders to meet project timelines Required qualifications Bachelor's degree in Statistics, Computer Science, Mathematics, Engineering, Life Science, or a related discipline 8-10+ years of programming experience in clinical trial data processing within the biotechnology, pharmaceutical, or CRO industries Proficiency in SAS programming, with knowledge of additional programming languages such as R or Python being a plus Strong understanding of CDISC standards and regulatory submission processes Experience in mentoring and managing teams in a programming environment
Manager, Statistical Programming in workfromhome at Unknown Company
This position is listed as full time and able to be worked remotely.