Senior Statistical Programmer

🔥 13 hours ago

🇧🇷 Brazil – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🖥 Software Engineer

👻 Ghost score 10%

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

• Perform the role of the Lead Statistical Programmer • Plan, execute, and oversee all programming activities on studies • Estimate resources, work within budget, meet timelines, maximize quality, and interact with departments and clients • Develop and maintain SAS programs to create SDTM and ADaM datasets and TFLs • Perform quality control of SDTM, ADaM, and TFL outputs • Produce Define XML/PDFs, Analysis Results Metadata (ARM), annotated CRFs, and Review Guides • Develop specifications for SDTM and ADaM datasets • Review SAPs and TFL shells from a programming perspective • Mentor less-experienced programmers on SDTM, ADaM, and TFL processes • Present and share knowledge at department meetings • Respond to QA and client audits and support qualification audits • Identify programming processes that improve productivity, quality, and efficiency • Perform other duties as needed or assigned

🎯 Requirements

• Bachelor’s degree, preferably in mathematics, statistics, computing, life science, health science, or related subjects • Experience and/or education plus relevant work experience equating to a Bachelor's degree • Relevant and equivalent experience may be accepted in lieu of educational requirements • Typically 3–5 years of SAS® programming experience in the CRO or Pharmaceutical industry, or equivalent combination of education and experience • Knowledge of CDISC requirements • English required for speaking, writing, and reading • Willingness and ability to travel locally, domestically, and regionally • Approximately 5% travel, with overnight stays potentially required for up to 100% of travel

🏖️ Benefits

• Remote work option • Office or home-based work environment • Travel to client meetings and trainings • Equal employment opportunity and accommodations support