Sr. Statistical Programmer (San Francisco) Two major pharmaceutical clients in San Francisco are looking to fulfill open SAS Programmer Positions to participate in upcoming clinical studies. Key Features -Serve as lead programmer and use professional concepts in accordance with company objectives to solve complex problems in creative and effective ways for one or more clinical studies. -Review and help develop documents related to study (Case Report Forms, Database Specifications, Statistical Analysis Plans, TLF specifications, etc). -Define analysis dataset specification and ensure that specifications are met. -Development of data definition tables based on analysis dataset specifications and company standards and policies. -Implement QA and QC validation in accordance with departmental SOP's for deliverables including: -Analyze and evaluate clinical data for completeness, correctness and consistency -Collaborate with statisticians and support programmer(s) on programming tasks and validation. -Participate in technical development and process improvement within Statistical Computing. -Develop, apply and promote consistent programming standards through standard processes and SOPs. -Work collaboratively with interdepartmental stakeholders (e.g., Clinical Operations, Drug Safety, Regulatory, Analytical Chemistry and Medical Affairs) to clarify program objectives, resolve issues, and gain efficiencies Requirements: -Minimum 5-8 years related experience. -Experience is within the pharmaceutical/biotech industry or relevant clinical research organization Industry -Experience in the development of analysis files and quality assurance of data -Experience in programming with a regulated environment -Experiences with Clinical Study Reports, NDA submissions and Oncology preferred -BS/BA/MS in Statistics, Computer Sciences, Mathematics, or Life Sciences. To be considered for this opportunity, please submit your resume immediately. Key Words - SAS, Sr. Programmer, Programmer, Clinical Data, CDISC
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