STATISTICAL PROGRAMMER

Major Biotech with a location in San Diego CA is seeking a SAS Programmer to join their team.

Requirements:
BS/ MS STATS , preferably in a scientific discipline such as Statistics, Mathematics, Economics. 5-10 years SAS Base programming, with 2-5 years using SAS STAT, GRAPH and MACRO· 5-10 years of clinical trial experience relevant experience in the pharmaceutical, biotechnology industry or CRO. Oncology Experience required.

Summary:
The Senior Statistical Programming Analyst III supports statistical programming activities in the production of Statistical Analysis Plan planned tables, listings and graphs, integrated summaries of safety and efficacy, ad hoc analyses and electronic submission deliverables such as datasets, data documentation, programs, programming table of contents, and patient profiles. This person is also responsible for monitoring and meeting assigned program milestones. May lead a small team of support statistical programmers to accomplish tasks, communicating issues as necessary to senior management.

Responsibilities:
Serves as SMT statistical programmer to achieve milestones; communicates issues or resource needs to senior management. Creates tables, listings, and graphs from specifications developed in conjunction with SMT statistician or support programming staff. Verifies that programs follow internal conventions and standards. Produces electronic submission components for regulatory submissions as appropriate. Reviews CRF SAS datasets and produce analysis datasets from specifications. Reviews CRF, database design, and edit check specifications from Clinical Data Management.·Assists senior management in establishing standardized programming procedures. Works with SMT or CDT statistician to develop a QC plan spanning multiple studies within a drug program. Able to provide QC for standard and non-standard tables, including efficacy.

Key Words: SAS, Data, STAT, Clin*, SAS, Prog*, Ad Hoc, SAS, California
REQUIREMENTS
MUST HAVE CLINICAL EXPERIENCE