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.
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