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Stat Programmer II

United States – RemoteClinical Development & Clinical OperationsRegular

Job Description

Statistical programmers work collaboratively with internal colleagues and external vendors to ensure the efficient, high-quality production of analysis datasets and statistical outputs for study reports and integrated summaries in support of Gilead’s regulatory, scientific and business objectives.

Key Skills

  • Shows effective collaboration with staff in Biostatistics, Clinical Data Management.
  • Begins to understand how to put together and update programming specifications.
  • Proactively anticipates the next steps for their work.
  • Programs Analysis Datasets, Table, Figure, Listings (TFLs) and ad hoc reports.

Job responsibilities

  • Works collaboratively with Clinical Development to meet study deliverables and timelines for statistical data analysis and reporting.
  • Assesses the quality of analysis data and performs cross-study analyses.
  • Uses internal macros to automate study deliverables.
  • Assists in submissions of electronic data (e.g., SAS® data sets) to regulatory agencies.
  • Has sufficient understanding to follow an analysis plan and provide programming support for study deliverables.
  • Assist in the review of GSI Policies, SOPs and other controlled documents
  • Provide input to and participate in Programming and Biometrics meetings.
  • Contribute to the continuous improvement of Programming Environment.
  • Excellent verbal and written communication skills and interpersonal skills are required.
  • Demonstrates SAS programming proficiency.
  • Has knowledge of clinical trial study design and electronic data submission requirements.

Education and experience

  • 4 years of experience and a BS degree in Biostatistics/Computer Science or equivalent.
  • 2 year of experience and a MS degree in Biostatistics/Computer Science or equivalent.