Senior Statistical Programmer
Core
Lead statistical programming for clinical studies, transforming complex clinical data into decision-ready evidence for global regulatory submissions.
Role type
Senior Statistical Programmer (Clinical Trials)
Builds
Clinical study datasets and analysis deliverables for regulatory submissions
Domain
Life Sciences / Clinical Development / Biostatistics
Required skills
SAS programming, SAS macros, CDISC standards, clinical development process knowledge, technical documentation, risk management, project management
Preferred skills
Experience across multiple therapeutic areas, experience with regulatory submissions
Technologies
SAS, R
Responsibilities
Lead programming deliverables for clinical studies, ensure quality and timeliness of outputs, implement statistical programming aspects of protocols, program independently with advanced techniques, write programming specifications and documentation, ensure adherence to CDISC standards, manage programming risks, collaborate with cross-functional teams, partner with contract programming providers, influence study strategies, plan and track programming aspects of projects
Seniority
Senior, hands-on IC
