
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.
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🕒 May 21
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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.
• Lead statistical programming teams to deliver on projects and communicate directly with the sponsor. • Oversee and/or be responsible for the quality and validation of statistical output produced. • Create or review SDTM and/or ADaM dataset specifications. • Program and/or validate SDTM and ADaM datasets, and TLFs. • Provide guidance and input on the statistical programmer requirements and queries during the conduct of the trial.
• B.Sc degree in Life / Computer Science, Statistics, or equivalent. • Minimum 5 years’ experience working as a Statistical Programmer. • Experience leading a team will be an advantage. • In-depth knowledge of either CDISC SDTM and/or ADaM standards. • Advanced knowledge of SAS, including SAS Macros. • Proven ability to program medium- to high complexity statistical output. • Excellent communication skills. • Prior oncology experience and/or team leadership experience is advantageous.
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