Senior Statistical Programmer

🕒 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 the Data Masters

WebsiteLinkedInAll Job Openings

51 - 200 employees

Founded 1998

🧬 Biotechnology

💊 Pharmaceuticals

☁️ SaaS

Biotechnology • Pharmaceuticals • SaaS

Bioforum the Data Masters is a biometric Contract Research Organization (CRO) that provides data-focused clinical development services to biotech and pharmaceutical sponsors. The company offers end-to-end clinical trial support including data management, biostatistics, statistical programming (SDTM/ADaM/TFLs), medical writing, project management, and regulatory submission support. Bioforum also develops analytics and validation tools—such as the BioGRID visualization platform with the AI assistant BRIAN, JetConvert for SDTM packages, and Validify for CDISC validation—positioning it as both a service provider and SaaS-enabled analytics vendor for clinical trial oversight and submissions. They serve startups, biotechs, and global pharmaceutical companies with FSP/rescue study models and expert-led solutions to optimize study design, data quality, and regulatory readiness.

📋 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