Senior Statistical Programmer FSP

Role Overview: As a Senior Statistical Programmer working fully embedded within a pharmaceutical client, supported by Cytel, you will play a crucial role in driving innovation and supporting global pharmaceutical clients in driving the next generation of patient treatment. You will have the opportunity to work autonomously and take ownership in a dynamic environment. Key Responsibilities: - Perform data manipulation, analysis, and reporting of clinical trial data using SAS programming - Generate and validate SDTM and ADaM datasets/analysis files, as well as tables, listings, and figures (TLFs) - Conduct production and QC/validation programming - Generate complex ad-hoc reports from raw data - Apply strong understanding/experience of Efficacy analysis - Create and review submission documents and eCRTs - Communicate with internal cross-functional teams and clients for project specifications, status, and inquiries - Lead duties when called upon - Be adaptable and flexible in response to changing priorities - Experience in Real-World Evidence (RWE) would be advantageous Qualifications: - Bachelor's degree in Statistics, Computer Science, Mathematics, or related fields - Minimum of 8 years of SAS programming experience with clinical trial data in the Pharmaceutical & Biotech industry with a bachelor's degree, or 6 years of experience with a master's degree or above - Study lead experience preferred, handling multiple projects simultaneously - Strong SAS data manipulation, analysis, and reporting skills - Proficiency in CDISC SDTM/ADaM standards - Strong QC/validation skills - Good ad-hoc reporting skills - Proficiency in Efficacy analysis - Familiarity with the drug development life cycle and clinical trial data analysis - Experience with submission documents and define.xml - Experience supporting immunology, respiratory, or oncology studies a plus - Excellent analytical and troubleshooting skills - Ability to deliver quality output within challenging timelines - Effective teamwork in a globally dispersed team environment - Experience in Real-World Evidence (RWE) would be an added advantage Additional Company Details: Cytel is the largest provider of statistical software and advanced analytics for clinical trial design and execution. With over thirty years of experience, Cytel's scientific rigor and operational excellence have helped biotech and pharmaceutical companies to navigate uncertainty and unlock the full potential of their data. Join a team where talent, experience, and scientific rigor collaborate to advance clinical development and contribute to the future of human health. Explore Cytel careers for opportunities in biostatistics, statistical programming, adaptive clinical trial design, and more.,