Sr Programmer Analyst (SAS and Clinical Data Experience Required)
Core
Lead programmer for moderately complex clinical trials studies, performing advanced bioinformatics programming, data management, and validation using SAS.
Role type
Senior IC clinical data programmer (SAS)
Builds
Validated programs, listings, tables, figures, and summary data for clinical research projects
Domain
Clinical trials / Pharmaceutical industry
Deliverable
production ML models | product features | dashboards & analysis
Required skills
SAS programming, data management across multiple systems, database structure knowledge, biostatistical metrics capture, quality control review, project timeline management, training and mentoring
Preferred skills
Experience with industry conferences, SOP development, bidding process support
Technologies
SAS
Responsibilities
Lead programming on moderate complexity studies, create/execute/validate data transfer and reporting programs, manage assignments to meet timelines, provide training to junior members, support departmental infrastructure and policies
Seniority
Senior, hands-on IC with lead responsibilities
