Description
Sr. SAS Programmer (Remote Location)A major pharmaceutical company in the greater Los Angeles is currently looking to fill 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:
-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 within 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 find out more about Real please visit www.realstaffing.com