Senior Statistical Programmer

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🕒 Novembro 25, 2025

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BioForum

SiteLinkedInTodas as Vagas

1 - 10 funcionários

Fundada em 2021

🧬 Biotecnologia

🤝 Sem Fins Lucrativos

🤝 B2B

Biotechnology • Non-profit • B2B

A BioForum é a Associação Polonesa de Empresas de Biotecnologia (Związek Firm Biotechnologicznych BioForum). Facilita o intercâmbio de informações, resultados de pesquisas e melhores práticas entre as empresas associadas, além de representar sua voz coletiva perante reguladores e formuladores de políticas em níveis nacional e europeu, defendendo políticas que apoiem a inovação em biotecnologia. A BioForum organiza conferências e eventos (CEBioForum, GreenBioForum), oferece treinamentos especializados, webinars e plataformas de networking (plataforma CEBioForum, banco de dados #POLISHBIOTECH), e colabora com agências governamentais, clusters industriais e organismos internacionais para promover o crescimento e a internacionalização do setor de biotecnologia da Polônia.

Descrição

• Participating in all statistical programming activities including preparing clinical data to submission using CDISC or customized standards. • Reviewing data conversions, data analysis datasets and outputs and taking part in creating best practices and implementation guides. • Might need to be responsible for project management (timelines, scope, budget, resourcing) on a project or program level. • Train, mentor and share knowledge with the rest of the statistical programming team. • Creating programming specification documents for all types of data (SDTM, ADaM, Derived data, etc.). • Might include Interaction with customers on a project or program level. • Development of SAS programs for conversion of the clinical data based on CDISC or customer instructions. • Development of SAS programs for analysis datasets based on SAP, shells and CDISC or customer instructions. • Development of SAS programs for study TFLs, based on study SAP and shells. • Review and verify all types of conversions and programming done based on customer requirements. • Development of core programs for validation, conversion, and maintenance of clinical data dataset structure. • Follow the appropriate Standard Operating Procedures (SOPs) for all statistical programming related activities.

🎯 Requisitos

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