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An opportunity has arisen for an experienced Senior/Principal Statistical Programmer to join a leading CRO, based from home in either the UK or Italy. This is a fantastic opportunity to work for a growing organisation that empowers its employees to work autonomously and creatively, to retain and develop the company’s Centre of Excellence for clinical data services. The Company Our client is a data-driven CRO that specialises in providing Biostatistics, Programming, Clinical Data Management, Medical Writing and Pharmacovigilance services alongside full-service solutions. Working for global pharmaceutical and medical device clients, the company supports large and small scale Phase I-IV drug development trials, offering a centralised clinical data approach alongside innovative technology solutions. Key Responsibilities • Coordinate and lead programming tasks at study level, including management of project budget, timelines and strategy • Support with the management and mentoring of junior colleagues • Production and validation of reliable statistical analysis using SAS • Programming CDISC structured datasets • Provide a professional interface with customers Skills and Experience required • Experience writing and reviewing database specifications, using CDISC standards • Experience of creating Define.xml and validation via OpenCDISC • Previous experience working in a CRO environment • Previous experience as a Lead Programmer on clinical studies • Substantial experience of programming datasets, tables, listings and figures using SAS from a Statistical Analysis Plan • Fluent in English To apply, please email your CV to [log in to unmask] Only candidates authorised to work in the EU may apply as sponsorship is not offered. You may leave the list at any time by sending the command SIGNOFF allstat to [log in to unmask], leaving the subject line blank.