Why PHASTAR? PHASTAR is a specialist CRO, offering statistical consulting, clinical trial reporting, data management and medical writing services, by providing expert consultants and managing and delivering in-house projects.

If you would like to work with a team of expert statisticians, in a company run and managed by statisticians, where your skills will be valued and nurtured, then our roles may be right for you. PHASTAR are a team of expert statisticians and programmers, working in the medical field.

There are a number of reasons you may wish to join the PHASTAR team:

  • Learn from PHASTAR’s internal experts and from personnel with specialist PhDs.
  • A better way to work: PHASTAR have a unique approach to statistical consulting and data analysis. Our approach ensures high quality consulting and data analysis.
  • A relaxed place to work. PHASTAR encourages a hard working but friendly and sociable office environment.

Job description:

  • Ability to lead a team of statisticians and programmers to manipulate, summarise and analyse clinical trial data using a variety of statistical methods, ultimately delivering clinical trial results to an agreed timeline with optimal quality
  • Project management responsibilities, including allocating staff, predicting and planning resources
  • Preparation and review of study documentation e.g. protocols and statistical analysis plans
  • Ability to advise, mentor and teach both internal and external statisticians with regards to statistical and data analysis methods
  • Function as a study expert across a number of studies, helping to clarify details on analysis methods for the internal PHASTAR team
  • Responsible for ensuring the team meets the highest quality standards, and follows the principles detailed in PHASTAR’s internal procedures
  • Maintaining a positive and engaging client relationship with regards to statistical issues


  • PhD or MSc in Biostatistics or related 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

What we 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)
  • Opportunities to get involved in the management of other statistical and programming staff members

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