Description
Leading global organisation requires a Statistician with Statistical Programming experience to work remotely from the UK with regular visits to their HQ in the Netherlands.This presents an exciting contract opportunity for a researcher within; epidemiology, health services research, biostatistics or a related quantitative subject.
Requirements:
- Conducting mixed treatment comparisons and patient level database statistical analyses.
- co-ordinating the statistical analysis of clinical projects
- Act as the main statistical contact for internal and external parties Designing , programming and interpretation of statistical and meta-analysis.
- Preparing documents and presenting statistical findings.
- Responsible for writing and reviewing analysis plans
- Responsible for writing and reviewing analysis plans
- Providing input into study design
- Programming in SAS
- Adhering to SOP's
- Ensuring the highest standards of GCP
Key requirements:
- Skills in statistics or quantative analysis of medical/biological data.
- MSc or PhD in Medical Statistics (or equiv)
- Significant experience in a clinical trials setting, ideally, within academia, 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
- Excellent communication and analytical skills.