Statistical Programming Contractor (16-Month Contract)

A 16-month statistical programming contract supporting clinical studies and regulatory submissions. The programmer develops and validates SAS analyses, creates CDISC datasets and prepares tables, figures and listings. The role collaborates with biostatistics, data management and clinical operations. Based in South Boston, Massachusetts, the employer describes a working arrangement with at least three onsite days per week.

Bachelor’s degree in statistics, mathematics or computing, with a master’s preferred. Requires at least three years of pharmaceutical, biotechnology or CRO statistical programming, hands-on SAS, SDTM and ADaM standards, and knowledge of clinical reporting and GCP/ICH requirements.