
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.
🕒 April 15
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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.
• Work as a principal programmer across multiple clinical and non-clinical studies • Supporting regulatory submission activities • Producing and validating datasets and outputs to excellent quality whilst adhering to deliverable timelines • Excellent knowledge of CDISC SDTM and ADaM implementation guidelines working independently in this area • Producing, reviewing and updating complex dataset specifications (including efficacy) • Creating and debugging complex macros • Reviewing Statistical Analysis Plans (SAPs) • Ensuring the principles in the PHASTAR checklist are followed rigorously • Act as a Lead programmer on multiple studies and project, ensuring quality and timely delivery
• Educated to BSc or above within Computer Science, Mathematics or a Science related discipline • SAS Programming Experience within the pharmaceutical industry and experience on Oncology Therapeutic Study • 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
• PHASTAR is committed to the principles and practices of equal opportunities and to encouraging the establishment of a diverse workforce.
Apply Now🕒 April 1
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