Senior Statistical Programmer – Sponsor Dedicated

Job not on LinkedIn

🕒 January 13

🌐 Poland, United Kingdom, +4 more countries – Remote

🇵🇱 Poland – Remote 🇬🇧 United Kingdom – Remote 🇸🇰 Slovakia – Remote 🇧🇪 Belgium – Remote 🇪🇪 Estonia – Remote 🇮🇪 Ireland – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 45%

What it means: how likely this posting is sitting open without active hiring.How to read it: 60% or higher means we think this is a ghost. Lower scores are less of a worry.How we score it: age, reposts, open roles vs team size, how fast jobs close, and whether pay is listed.Fine print: an estimate from public data, not a judgment of the company. Real jobs can score high, so treat it as a hint, not a fact.

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Fortrea

WebsiteLinkedInAll Job Openings

10,000+ employees

🏥 Healthcare

🧬 Biotechnology

💊 Pharmaceuticals

Healthcare • Biotechnology • Pharmaceuticals

Fortrea is a global clinical research organization (CRO) specializing in providing comprehensive clinical development services to biopharma and MedTech companies. With over 30 years of experience, Fortrea offers a range of services including clinical pharmacology, phase I-IV study management, regulatory strategy, market access, and more. They focus on advancing healthcare innovation by integrating data and scientific expertise to deliver tailored solutions that enable faster decision-making and improve patient outcomes, especially in the realm of cell and gene therapy programs, as well as various therapeutic areas like oncology, cardiovascular, and infectious diseases.

📋 Description

• Review SAPs and TFL shells from a programming perspective. • Advise on the development of complex TFL shells from a programming perspective. • Develop and/or lead the development of complex specifications for SDTMs and ADaM datasets. • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs, and perform quality control of SDTM, ADaMs and TFLs. • Produce / define XML / PDFs, Analysis Results Metadata (ARM), aCRFs and Reviewers Guides to support SDTMs and ADaMs. • Respond to QA and client audits and support qualification audits. • Identify and propose innovative ways to improve the efficiency, quality and productivity of our clinical statistical programming business.

🎯 Requirements

• Degree in a relevant field such as mathematics, life sciences, statistics, computer sciences, etc. • Solid professional experience as a statistical programmer within a biotech, CRO or pharmaceutical company. • Demonstrated knowledge of base SAS, SAS macros, SAS/STAT; demonstrated ability to debug SAS programs. • Proven professional experience with SDTMs, ADaM datasets (safety and efficacy) and TFLs. • Solid knowledge of CDISC standards. • Business fluency in English – both spoken and written – is a must.

🏖️ Benefits

• Flexible work arrangements • Professional development opportunities