Meet Life Sciences

Senior Statistical Programmer Remote (US-based) Full-time Permanent We're partnering with a well-established, global clinical research organisation that provides full-service support to the pharmaceutical, biotechnology, and medical device industries. With a strong reputation for quality, flexibility, and customer focus, they are continuing to expand and are now seeking a Senior Statistical Programmer to join their growing team. This is an opportunity to contribute to high-impact clinical trials within a collaborative, technically driven environment, working on innovative therapies and advancing global healthcare. The Role As a Senior Statistical Programmer, you will be responsible for the design, development, and validation of clinical trial datasets and outputs, ensuring compliance with industry standards and sponsor requirements. You will play a key role in delivering high-quality programming outputs across studies, while also supporting and mentoring junior team members and contributing to process improvement initiatives. Key Responsibilities Design and specify study data tabulation models and analysis data models (e.g. SDTM, ADaM) Develop and validate datasets in line with industry standards and study requirements Program and generate statistical outputs and reports using SAS Independently validate outputs and datasets created by other programmers/statisticians Develop and test SAS code for data checks and ongoing data review Ensure all programming documentation is accurate and compliant with SOPs Support data archiving activities in line with regulatory requirements Provide technical guidance and mentorship to junior programmers Contribute to the development of programming standards and best practices Support continuous improvement initiatives within statistical programming Requirements Master's degree in Mathematics, Statistics, or a related field Minimum 5+ years' experience in statistical programming within clinical trials Strong expertise in SAS programming Experience working with clinical trial datasets and regulatory standards Strong understanding of data structures and statistical reporting Ability to work independently and collaboratively in a global team Excellent attention to detail and problem-solving skills Experience mentoring or supporting junior colleagues is advantageous What's on Offer Fully remote working within the US Opportunity to work with a leading global CRO Exposure to a wide range of therapeutic areas and global studies Supportive, collaborative, and growth-oriented environment Strong focus on quality, innovation, and professional development If you're an experienced Statistical Programmer looking to take the next step in your career within a high-quality, globally recognised CRO, we'd love to hear from you. Apply now or get in touch for a confidential conversation.