Topic: statistical programming

Lead biostatistics and the wider biometrics function for Prime Medicine’s gene editing clinical programmes. The role develops trial designs, endpoints, dose-escalation strategies and analysis plans while overseeing clinical data management and statistical programming partners. It supports regulatory interactions and quantitative decisions from protocol development through submission, and builds the organisation’s biometrics capabilities in Cambridge, Massachusetts.

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.