Fortrea
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
Senior Statistical Programmer – Oncology
Job not on LinkedIn
18 hours ago
Fortrea
Biotechnology • Pharmaceuticals • Healthcare Insurance
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
• Perform programming activities for oncology clinical trials • Review SAPs and TFL shells from a programming perspective • Advise on design and development of TFL shells and statistical outputs • Develop specifications for SDTM and ADaM datasets • Produce and validate Define.xml/PDFs and regulatory submission packages
🎯 Requirements
• Degree in Mathematics, Life Sciences, Statistics, or Computer Science • Minimum of 4 years’ hands-on experience in oncology clinical trials • Proven experience with SAS programming (Base SAS, SAS Macros, SAS/STAT) • Strong practical knowledge of CDISC standards (SDTM, ADaM) • Experience with regulatory submission deliverables (Define.xml, ARM) • Business fluency in English, both spoken and written
🏖️ Benefits
• 100% home-based or local office work option • Impactful role in oncology treatment development
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