Sr Programmer Analyst
Core
Lead programmer for moderately complex clinical trials studies, developing and validating statistical programs to manage data across multiple systems and generate reports/tables/figures.
Role type
Senior IC statistical programmer (clinical trials)
Builds
Statistical programs, data listings, tables, and figures for clinical research projects
Domain
Clinical trials / Pharmaceutical industry
Required skills
SAS programming, data management across multiple systems, relational database structure, biostatistical metrics capture, quality control review, training and mentoring
Preferred skills
Advanced bioinformatics programming, statistical and computational considerations
Technologies
SAS
Responsibilities
Lead programming on moderately complex studies, create/execute/maintain/validate data transfer and reporting programs, manage assignments to meet timelines, provide training and guidance to junior members, support bidding processes
Seniority
Senior, hands-on IC
