Description
CSL Seqirus is hiring a Senior Clinical Statistical Programmer to take technical ownership of one or two clinical trials from study setup through regulatory submission. The role involves interpreting protocols and data specifications, designing and validating SDTM and ADaM datasets, leading integrated analyses, reviewing CRO deliverables, mentoring programmers, and supporting regulatory queries and publications. It requires pharmaceutical or clinical research programming experience, strong SAS proficiency, CDISC knowledge, submission-ready dataset experience, and regulatory submission experience, with a BSc in a relevant field. The position is hybrid, requiring three days per week onsite in Maidenhead.
