Phastar
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.
Senior/Principal Programmer
Job not on LinkedIn
November 25
Phastar
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.
đź“‹ Description
• Support regulatory submission activities • Produce and validate datasets and outputs • Program and validate datasets and SDTMs • Become independent technical expert • Perform Senior Review and Deliver QC of non-statistical output • Develop and implement standard macros • Validate and perform User Acceptance Testing on macros • Create, QC and update complex dataset specifications • Provide consultancy, advice and training on SDTM and ADaM standards • Initiate projects for programming development • Ensure study compliance with SOPs 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
• flexible working • part-time hours • involvement in developing company-wide initiatives • structured training and development plans • supportive, fun and friendly environment • tree planting in your honour as part of ESG initiatives
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