What are the responsibilities and job description for the Clinical SAS Manager / Programmer #3483818 position at Axiom Path?
Be Part of a High-Performing TeamThis opportunity supports a leading organization in the pharmaceutical and biotechnology sector known for driving innovative clinical development and maintaining a collaborative, data-driven culture. The team operates within a highly technical environment that values scientific rigor, precision, and reliable execution. With seasoned experts across biostatistics, clinical operations, and data management, the group emphasizes quality, continuous improvement, and efficient delivery across all phases of clinical research. The environment is fast-paced, structured, and ideal for individuals who thrive in technically demanding settings where their work directly supports regulatory and clinical success.What’s In Store For YouOpportunity to lead complex programming work within a scientifically rigorous environment.Engage directly with cross-functional teams and contribute to high-visibility clinical initiatives.Work on-site in a collaborative setting that encourages knowledge sharing and technical excellence.Grow your experience in a setting that values innovation, problem-solving, and data accuracy.How You Will Make an ImpactLead programming efforts supporting clinical studies and regulatory deliverables.Develop and validate SDTM and ADaM datasets in alignment with CDISC standards.Produce high-quality analysis outputs, including tables, listings, and figures for trials and publications.Create, maintain, and optimize SAS macros and utilities to enhance programming efficiency.Draft clear dataset specifications aligned with study protocols and analysis plans.Partner with statisticians, data managers, and clinical teams to ensure accurate, timely outputs.Manage multiple complex assignments and drive them to completion with minimal oversight.Contribute technical expertise to problem-solving, workflow enhancements, and process improvements.Are you a proven statistical programming professional ready to make an impact?Required Skills & Experience10 years of clinical or statistical programming experience within pharma, biotech, or related industries.Advanced SAS programming skills with demonstrated expertise in dataset creation and validation.Deep familiarity with CDISC SDTM and ADaM standards.Prior leadership experience supporting studies or overseeing programming deliverables.Strong understanding of clinical trial data structures and regulatory expectations.Excellent communication skills and ability to collaborate across cross-functional teams.Bachelor’s degree in Statistics, Computer Science, Mathematics, or a relevant scientific discipline.Preferred ExperienceHands-on involvement in regulatory submission activities.Experience with R, Python, S-Plus, WinBUGS, C , or VBA.Background supporting exploratory or publication-driven analyses.Knowledge of broader statistical software and emerging programming tools.#dice
