Senior Statistical Programmer - UK (Remote/Office/Hybrid) - #1776347

• Perform consistency review of clinical trial documents including protocols, SAPs, CRFs, CSRs


• Author and review simple and complex study TFL shells


• Author and review simple and complex dataset standards


• Perform data checks and data exploration (e.g. using frequencies, histograms)


• Program and QC routine and ad hoc datasets and TFLs (in SAS) following specifications, applying good programming practice


• Complete and review CDISC Validation tool reports


• Ensure the appropriate standards are being applied and adhered to


• Familiarisation with simple statistical techniques (e.g. t-test, ANOVA, regression, standard survival)


• Review of project management related documents


• Maintain study master file documents and any other documents that are required to be audit ready

General

• Lead internal and client study team meetings effectively


• Present study updates internally and at client meetings


• Share scientific, technical and practical knowledge within the team and with colleagues


• Perform work in full compliance with applicable legislation, regulations, company policies, procedures, and training


• Build effective collaborative working relationships with internal and client team members


• Seek opportunities to develop innovative ideas, sharing when appropriate


• Line management or mentorship of more junior team members


• Contribution to development of internal training materials


• Contribution to internal process improvement initiatives

Minimum Qualification Requirements

• BSc, MSc or PhD in numerical discipline (or relevant equivalent industry experience)


• At least 4 years of relevant industry experience