Senior Analyst, Statistical Programming
Core
Develop complex analysis datasets, specifications, and summary output (tables, listings, or graphs) for clinical reports using statistical programming languages to support Transcatheter Mitral and Tricuspid Therapies business outcomes.
Role type
Senior IC statistical programmer (clinical trials)
Builds
Clinical reports and regulatory-compliant analysis datasets for medical device/therapies
Domain
Medical device / Cardiovascular / Clinical trials
Required skills
SAS, R, statistical programming, clinical data management (CDM), regulatory guidelines (GCP, ICH, FDA, ISO), complex data analysis, program validation
Preferred skills
MS Office Suite integration with SAS, clinical trial experience in pharma/medical device, leadership, stakeholder coordination
Technologies
SAS, R, MS Office Suite
Responsibilities
Develop complex analysis datasets and specifications; Create and validate statistical programs; Review and validate programs against regulatory standards; Perform complex analysis in response to data requests; Collaborate with CDM and statisticians on CRF and database specifications
Seniority
Senior, hands-on IC
