Sr Programmer Analyst II
Core
Lead Programmer or Study Lead managing end-to-end clinical SAS programming for complex clinical research projects.
Role type
Senior IC clinical SAS programmer (Study Lead)
Builds
CDISC-compliant clinical datasets (SDTM, ADaM) and Tables, Listings, and Figures (TLFs)
Domain
Clinical research / Biopharmaceuticals
Required skills
SAS programming (Base SAS, Macros, PROC SQL), CDISC standards (SDTM, ADaM), TLF development, clinical trial processes, regulatory compliance, study lead management, mentorship
Preferred skills
Relational databases, process improvement, resource planning
Technologies
SAS, CDISC
Responsibilities
Lead programming activities for complex clinical studies, develop and validate SAS programs for data analysis, ensure compliance with CDISC standards, collaborate with cross-functional teams, mentor junior programmers, manage project timelines and deliverables
Seniority
Senior, hands-on IC with leadership responsibilities
