Statistical Programmer

reliable analytical outputs.What You Will Be DoingDesigning, developing, and validating SAS programs to support statistical analysis and reporting across multiple clinical studies.Leading the creation, validation, and documentation of SDTM and ADaM datasets, ensuring strict adherence to CDISC standards and regulatory expectations.Collaborating closely with biostatisticians to develop robust statistical analysis plans and implement appropriate statistical methodologies.Performing high-quality review and quality control of statistical outputs, ensuring accuracy, consistency, and compliance with study specifications and regulatory guidelines.Supporting the preparation of analysis summaries, statistical reports, data presentations, and materials for regulatory submissions.Mentoring and guiding junior programmers, sharing expertise, and promoting best practices within the programming team.Working in close partnership with sponsor teams within the FSP model, contributing to efficient workflows

knowledge sharing, and project delivery.Your ProfileBachelor's or Master's degree in Statistics, Mathematics, Computer Science, or a related discipline.Extensive experience in statistical programming within the pharmaceutical, CRO, or biotech industry.Strong hands-on experience with SDTM and ADaM dataset development and validation.High proficiency in SAS programming, with a solid grounding in statistical concepts and clinical data structures.Excellent analytical, problem-solving, and organizational skills, with the ability to manage multiple priorities in a fast-paced environment.Strong communication and interpersonal abilities, with a collaborative mindset suited to working with multidisciplinary project teams, including embedded sponsor colleagues.What ICON Can Offer You Our success depends on the quality of our people. That's why we've made it a priority to build a diverse culture that rewards high performance and nurtures talent.In addition to your competitive salary, ICON

Senior Statistical ProgrammerICON plc is a world-leading healthcare intelligence and clinical research organization. We're proud to foster an inclusive environment driving innovation and excellence, and we welcome you to join us on our mission to shape the future of clinical development.Join ICON as a Senior Statistical Programmer II and take your career to the next level by working directly with one of our major global biopharma partners through an embedded Functional Service Provider (FSP) model. This opportunity gives you the benefits of ICON's supportive, collaborative environment while working closely with a world-leading sponsor on impactful clinical research programs.In this role, you will play a critical part in the analysis and reporting of clinical trial data, ensuring scientific rigor, compliance, and high-quality deliverables. You'll contribute to the advancement of global clinical studies by developing complex statistical programs, validating key datasets, and shaping, A leading clinical research organization in Livingston is seeking a Senior Statistical Programmer to analyze and report clinical trial data. In this role, you'll design and validate SAS programs, lead creation of SDTM and ADaM datasets, and collaborate with...