Statistical Analyst
2 days ago
Key ResponsibilitiesWe develop, validate, and maintain datasets, transforms, and analytical outputs for clinical trials.We support oncology studies by ensuring accuracy, consistency, and regulatory compliance in all programming deliverables.We contribute to integrated summaries of safety and efficacy activities, including dataset integration, analysis, and documentation.We work closely with statisticians, data managers, and clinical teams to ensure timely and quality delivery.We assist in regulatory submissions and queries, providing clear, traceable, and compliant programming outputs.We collaborate in an agile environment, participating in planning meetings, sprints, and continuous improvement discussions.We work with internal tools and platforms, following established standards and governance.We troubleshoot data/programming issues and propose process enhancements.We ensure adherence to CDISC standards, good programming practices, and audit-ready documentation.Required Skills & Qualifications4-14 years of industrial experience.Proficiency in R programming language.Solid experience in SAS programming, especially in a clinical/biostatistics environment.A good understanding of CDISC standards and clinical trial data flow.Strong problem-solving skills, attention to detail, and ability to work in cross-functional teams.BenefitsThe opportunity to work on impactful research projects with global teams.A continuous learning and upskilling environment.A collaborative, agile work culture.Exposure to the end-to-end statistical programming lifecycle and regulatory submissions.About Our TeamWe prioritize collaboration and teamwork.We value continuous learning and professional growth.We strive for excellence in our work and services.
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