Senior & Principal Programmers

SUMMARY As a Senior Programmer, you will work across clinical and non‑clinical trials, delivering high‑quality programming outputs within agreed timelines. You will apply deep knowledge of CDISC SDTM and ADaM, interpret SAPs and output shells, develop macros, and support study‑level programming leadership. You’ll also act as a key technical contact, supporting junior team members and influencing best practices across studies. RESPONSIBILITIES Program and validate SDTM datasets, including complex efficacy and laboratory domains Program complex non‑efficacy outputs and figures Develop, debug, and maintain complex SAS macros Create, QC, review, and update complex dataset specifications across single and multiple studies Independently review SAPs (simple study designs) and output shells, providing feedback Apply SDTM and ADaM standards consistently and correctly Lead the creation and delivery of Clinical Regulatory Trial (CRT) packages, including define.xml / define.pdf Act as a point of contact for programming issues and ensure team alignment Liaise with Study Statisticians and Project Managers on resourcing and deliverables Take ownership of study-level resources and timelines Support internal training and contribute to programming development initiatives Ensure compliance with SOPs, internal checklists, and documentation archiving standards KEY EXPERTISE & COMPETENCIES Strong written and verbal communication skills Collaborative team player with a positive, proactive mindset Strong problem‑solving skills and attention to detail Ability to manage competing priorities and make timely technical decisions Strong understanding of regulatory requirements Proactive in identifying and resolving study‑level issues Open to feedback