Senior Statistical Programmer

Job not on LinkedIn

🕒 November 25, 2025

🇺🇸 United States – Remote

⏰ Full Time

🟠 Senior

🖥 Software Engineer

👻 Ghost score 85%

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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BioForum

WebsiteLinkedInAll Job Openings

1 - 10 employees

Founded 2021

🧬 Biotechnology

🤝 Non-profit

🤝 B2B

Biotechnology • Non-profit • B2B

BioForum is the Polish Association of Biotechnology Companies (Związek Firm Biotechnologicznych BioForum). It facilitates exchange of information, research results and best practices among member companies, represents their collective voice to regulators and policymakers at national and European levels, and advocates for policy supporting biotechnology innovation. BioForum organizes conferences and events (CEBioForum, GreenBioForum), provides specialized training, webinars and networking platforms (CEBioForum platform, #POLISHBIOTECH database), and collaborates with government agencies, industry clusters and international bodies to promote the growth and internationalization of Poland’s biotech sector.

📋 Description

• Participate in all statistical programming activities, including preparing clinical data for submission using CDISC or customized standards • Review data conversions, analysis datasets, and outputs • Contribute to creating best practices and implementation guides • Manage project or program-level timelines, scope, budget, and resourcing as needed • Train, mentor, and share knowledge with the statistical programming team • Create programming specification documents for SDTM, ADaM, derived data, and other data types • Interact with customers at the project or program level as needed • Develop SAS programs for clinical data conversion based on CDISC or customer instructions • Develop SAS programs for analysis datasets based on SAP, shells, and CDISC or customer instructions • Develop SAS programs for study TFLs based on study SAP and shells • Review and verify conversions and programming against customer requirements • Develop core programs for validation, conversion, and maintenance of clinical data dataset structures • Follow appropriate SOPs for statistical programming activities

🎯 Requirements

• Minimum 6 years’ experience as a statistical programmer working on clinical trials • Good knowledge of TFL programming • Experience programming according to CDISC standards, including SDTM and ADaM • Experience preparing submission documents, including Reviewer’s Guide and Define.xml • Bachelor’s degree in statistics, computer science, or a life science discipline • Attention to detail • Excellent communication skills