Ready for your next career move? With continued business growth and a strong pipeline of new projects, Veramed is creating new opportunities for Statistical Programmers to work on innovative studies, expand their skills and advance their careers within a supportive, specialist CROWe have multiple exciting opportunities for Principal and Senior level Statistical Programmers skilled in SAS and R, to join us on a permanent basis. We can offer fully remote, hybrid or office-based working, training and a very supportive and quality focused environment.The purpose of the role is to provide programming support to the statistics and programming department across a range of projects, clients and therapeutic areas. The Senior or Principal Programmer may also perform a supervisory role (e.G. line management and/or project management).Key ResponsibilitiesTechnical
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Previous experience with SAS and some R experience/knowledge.
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Perform review of clinical trial documents including protocols, SAPs, CRFs, CSRs
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Author, review and approve study TFL shells and dataset specifications
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Author,



validate and document SAS programs for datasets, TFLs and macros, applying goodprogramming practice
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Identify data issues and outliers
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Complete, review and approve CDISC Validation tool reports
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Identify data and standards issues and resolve or escalate as appropriate
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Awareness of emerging standards and associated impact to ongoing and future planned trials
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Maintain proficiency in SAS and awareness of developments
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Maintain study master file documents and any other documents that are required to be audit readyGeneral
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Lead internal and client study, project and cross functional team meetings effectively
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Present study updates internally and at client meetings
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Share scientific, technical and practical knowledge within the team and with colleagues
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Perform work in full compliance with applicable internal and client policies, procedures, processesand training
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Build

📌 Principal Or Senior Statistical Programmer (Madrid)
🏢 Veramed
📍 Madrid