Principal Statistical Programmer - FSP
City of London, Greater London, UK
Hybrid / WFH Options
Hybrid / WFH Options
Proclinical Staffing
an EU passport. Responsibilities: Evaluate clinical trial documents such as protocols, SAPs, CRFs, and CSRs. Author, review, and approve study TFL shells and dataset specifications. Develop, validate, and document SAS programs for datasets, TFLs, and macros following best practices. Identify and resolve data issues, outliers, and standards discrepancies. Review and approve CDISC validation tool reports. Stay updated on emerging … projects, including resource management, risk assessment, and delivery to budget. Lead internal and client meetings, share knowledge, and contribute to process improvement initiatives. Key Skills and Requirements: Proficiency in SAS programming with experience in clinical trial disclosures and/or data anonymization. Familiarity with CDISC standards (SDTM, ADaM) and TLF generation. Strong problem-solving skills and ability to apply More ❯
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