Biostatistical Programmer - Work from Home / Remote

This position offers an opportunity to assist in building a biostatistics department at Atlantic Research Group.   Open and direct verbal and written communication skills are required.  The incumbent of this position will work from our headquarters in Charlottesville, VA (for the right candidate, a remote / home based capacity will be considered). 

Description
  • Program mapped and analysis datasets per CDISC standards, tables, listings, and figures and other programming activities in a timely manner
  • Perform quality control review of programming activities to ensure that outputs meet quality standards and project requirements
  • Create and maintain statistical programming project documentation, including: project documentation, testing, and verification/quality control documents and programs
  • Negotiate and establish accurate time estimates for completion of study programming activities with internal team members and Biostatistical Management
  • Direct the programming activities of other programming personnel and monitor progress on programming deliverables
  • Be knowledgeable of  industry regulations
  • Program efficiently and accurately in SAS
  • Act as resource for SAS programming within organization
  • Participates in a highly collaborative environment as an integral member of a clinical project team to create data displays and data summaries for studies
  • Serves as a supporting programmer on multiple projects
  • Ability to collaborate effectively with non-statisticians and project managers, to work independently with minimal guidance, and as part of a team
  • Effective oral and written communication and interpersonal skills

Qualifications
  • Bachelor’s degree in Biology, Biotechnology, Mathematics, Statistics, Computer Science, or a related field plus 2 years of experience as Bio-Statistical/Analysis Programmer with clinical trial experience.
  • Proficient knowledge of SAS/BASE, SAS/SQL, SAS/STAT, SAS GRAPH, and SAS Macro Language
  • Programming or producing analysis datasets, summary tables, data listings and graphical representations of clinical trials data 
  • Using clinical regulatory guidelines (FDA/CFR, ICH/GCP, CDISC) in programming decisions
  • Statistical programming or reports in Phase I-III clinical trials utilizing SAS Programming (SAS/Base, SAS/Stat, SAS/Graph, SAS/SQL);

  • Application of CDISC guidelines mapping data to SDTM and ADaM formats required

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