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Title:SAS Programmer
Salary:Open
Experience:3-5
Location:MD - Rockville

Description:
The Programmer will support Biostatisticians and the Clinical team in analysis and presentation of study information.

Responsibilities:
  • Understand the reporting and data cleaning needs for clinical studies, and create suitable and representative Tables, Listings and Figures
  • Design and develop project-specific SAS programs for biostatisticians and Product Safety, often producing analysis datasets
  • Development of utilities for QC/QA and analyses
  • Assist in data review process, developing presentations and integrated computer programs to assist in the data review process and to provide operational metrics on resources and timelines
  • Assist in creation and management of an integrated and reusable programming suite, primarily in SAS, for use across multiple projects
  • Participate in study team meetings providing contact for assigned study related SAS programming activities and deliverables
  • Assist in data retrieval from Oracle Clinical, vendors and other sources
  • Recommend and participate in overall process improvements for programming
  • Assist in the development of guidelines and workflows for programming activities
  • Assist with other departmental tasks and responsibilities as needed

Requirements:
  • Bachelors degree in Computer Sciences, Statistics, Mathematics, or relevant scientific discipline
  • A minimum of 5 years experience in SAS Programming, with 3 years experience in biologics/drug development
  • Experience in data cleaning or biostatistics is a plus
  • Proven success in the development, documentation and qualification of programs to generate data presentations (Tables, Listings and Figures) for Clinical Studies using base SAS, SAS MACRO and GRAPH, SQL, and using ODS for presentations and data mining reports
  • Experience with data transfer, cleaning and validation techniques to provide single and multi-study integrated datasets; strong quantitative and analytical skills, with the ability to identify problems in complex algorithms and provide working solutions
  • Must have a high level of attention to detail
  • Demonstrated knowledge and understanding of programming standards and methodologies, GCP, ICH, CDISC and related FDA regulations
  • Ability to manage and prioritize multiple tasks concurrently
  • Experience with Oracle Clinical, Integrated Review, or other relational data management software is considered a plus
  • Experience with EDC data and products and is considered a plus

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