In this role you will be the sole statistician on a global outsourced, observational research project working side by side with the Head of Project Management. In this role you will:
· co-ordinate the statistical analysis of assigned clinical projects
· act as the main statistical contact for internal and external parties (including the steering committee)
· responsible for writing and reviewing stats analysis plans (SAP)
· provide input into study design
· program in SAS on an ad hoc basis
· adhere to client SOP's
· ensure the highest standards of GCP
Qualifications and Experience
· MSc or PhD in Medical Statistics (or equiv)
· Significant experience in a clinical trials setting, ideally, within CRO or Pharma.
· Excellent written and spoken English and posses the right to work in the UK.
· Experience within late phase, observational research would be an advantage
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