Sr Programmer Analyst
Core
Lead programmer for moderately complex clinical trials studies, developing and validating SAS programs to transfer, combine, and analyze data across multiple systems for pharmaceutical research.
Role type
Senior IC statistical programmer (clinical trials)
Builds
Validated statistical programs, data listings, tables, and figures for clinical studies
Domain
Pharmaceutical industry + clinical trials
Required skills
SAS programming, data management across multiple systems, relational database structure, biostatistical metrics capture, quality control review, project timeline management, training and mentoring
Preferred skills
None stated
Technologies
SAS
Responsibilities
Lead programming on moderately complex studies, create/execute/maintain/validate data transfer and analysis programs, manage assignments to meet timelines, provide training and guidance to junior members, support bidding processes
Seniority
Senior, hands-on IC