Statistical Programmer

vor 1 Woche


City of Melbourne, Österreich Xprt Dev Vollzeit

Senior & Principal Statistical Programmer (SAS) | Clinical Trials | Remote Australia Ready to own complex programming for global studies while still having real influence in a tight‑knit team? This permanent role is ideal for experienced Clinical SAS Programmers who want technical depth, autonomy, and direct impact on oncology development. The Company (Boutique, Full‑Service CRO) Mid‑sized, full‑service CRO with offices in Sydney and North America, running Phase I–IV trials for innovative biotech and pharma sponsors. Known for senior, hands‑on leadership, short decision lines, and genuine collaboration between biometrics, clinical operations, and medical writing. Strong presence in Australia with a growing biometrics function, giving visibility, influence, and opportunities to shape processes and best practices. The Role Permanent Senior and Principal Statistical Programmer positions, fully remote anywhere in Australia. Lead and deliver SAS programming across global oncology trials, partnering closely with two major pharma sponsors on their portfolios. Take ownership of end‑to‑end deliverables: dataset programming (incl. SDTM/ADaM), TLFs, quality checks, and contribution to analysis and reporting strategy. What You’ll Do Develop, validate, and maintain robust SAS programs for clinical trial data (SDTM, ADaM, TLFs) in line with CDISC standards. Design and optimise macros, automate workflows, and improve efficiency across multiple complex studies. Work closely with biostatisticians, data management, and study teams to ensure high‑quality outputs for CSRs and regulatory submissions. Mentor junior programmers (for Principal level) and contribute to programming standards, templates, and best practices. Why It Appeals to Experienced Programmers High technical bar: challenging oncology studies, advanced CDISC work, and meaningful macro development rather than just production coding. Real influence: your ideas on tooling, standards, validation strategies, and automation will actually be implemented. Stability with variety: permanent role with the project diversity of a CRO—different sponsors, indications, and phases. Culture: senior, experienced peers; pragmatic processes; and leadership that understands biometrics and gives programmers a voice. Competitive salary package with annual bonus, plus flexibility and remote‑first working. Ideal Profile 4+ years’ statistical programming experience in clinical trials (Senior) and significantly more for Principal level. Strong SAS programming, macro development and deep CDISC SDTM/ADaM knowledge. Solid oncology experience is essential; global trial experience highly regarded. Comfortable leading deliverables, collaborating across functions, and communicating clearly with internal teams and sponsors. Location: Remote Australia & New Zealand Pay rate: Negotiable #J-18808-Ljbffr



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