Principal Statistical Programmer
Principal Statistical Programmer

Principal Statistical Programmer  - Phastar

Based in either London, Macclesfield, Kent or Glasgow

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


We can offer:

  • Advancement of your career in an intellectually-stimulating, dynamic, supportive environment
    Variety of projects in statistical consultancy and clinical trial reporting (range of therapeutic areas and phases)

  • Excellent remuneration (competitive salary, pension, healthcare, conferences and courses etc)

You should be eligible to work in the UK. To apply, please send your details to or phone +44 (0)20 7183 7061