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Based in either RTP (NC, US)

Principal Statistical Programmer

in US - North Carolina
Start date: As soon as possible
Role and responsibilities

Key Requirements

  • Responsibility for overall project delivery, including clinical trial reports and other regulatory submission deliverables
  • Project management responsibilities, including allocating staff, predicting and planning resources
  • Act as a study expert for a number of studies, with an ability to clarify details on analysis methods for the internal PHASTAR team
  • Advise on internal, client and CDISC data standards
  • Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in PHASTAR's internal procedures
  • Function as a programming expert across a number of studies
  • Maintaining a positive and engaging client relationship with regards to statistical and/or programming issues
  • Report on study progress to the PHASTAR management team

Candidate Requirements

  • Educated to degree level or equivalent within a relevant discipline.
  • Experience working within a clinical trials environment (Pharma, CRO or academic)
  • Previous experience performing statistical analysis using SAS
  • Excellent written and verbal communication skills

You should be eligible to work in the US for this position. To apply, please complete the form below.

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