In this role within clinical research, you will:
· co-ordinate the statistical analysis of clinical projects
· act as the main statistical contact for internal and external parties
· responsible for writing and reviewing analysis plans
· provide input into study design
· program in SAS
· adhere to 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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