Phastar
201 - 500 employees
Founded 2007
💊 Pharmaceuticals
🧬 Biotechnology
🤝 B2B
Pharmaceuticals • Biotechnology • B2B
Phastar is a global biometrics contract research organization (CRO) that provides end-to-end clinical data solutions, including biostatistics, statistical programming, data management, data science, and data visualization to support clinical trials and regulatory submissions. The company offers flexible, scalable delivery models (project-based and functional service partnerships), proprietary frameworks and analytics tools to prepare high-quality, submission-ready data, and emphasizes a right-first-time approach and regulatory-first quality standards to accelerate drug development.
Programming Manager
🕒 May 2
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Phastar
201 - 500 employees
Founded 2007
💊 Pharmaceuticals
🧬 Biotechnology
🤝 B2B
Pharmaceuticals • Biotechnology • B2B
Phastar is a global biometrics contract research organization (CRO) that provides end-to-end clinical data solutions, including biostatistics, statistical programming, data management, data science, and data visualization to support clinical trials and regulatory submissions. The company offers flexible, scalable delivery models (project-based and functional service partnerships), proprietary frameworks and analytics tools to prepare high-quality, submission-ready data, and emphasizes a right-first-time approach and regulatory-first quality standards to accelerate drug development.
📋 Description
• Work as an experienced programmer across multiple clinical studies • Support regulatory submission activities • Produce and validate datasets and outputs • Program and validate datasets and SDTMs • Program complex non-efficacy outputs/figures • Perform Senior Review and Deliver QC of non-statistical output • Coordinate and perform code reviews • Create, QC and update complex dataset specifications • Act as a Lead programmer on multiple studies and projects • Develop archiving systems and processes
🎯 Requirements
• Educated to BSc or above within Computer Science, Mathematics or a Science related discipline • SAS Programming Experience within the pharmaceutical industry • Good awareness of clinical trial issues, design, and implementation • Experience of regulatory submissions and associated industry guidance • Familiarity with GCP and regulatory requirements • Knowledge of SDTM and ADaM CDISC standards
🏖️ Benefits
• Professional development opportunities • Equal opportunities employer • Support for diversity in workforce
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