Statistical Programmer

2 weeks ago

Oxfordshire, United Kingdom Nicholas Howard Full time

Nicholas Howard is delighted to be working with an innovative Clinical Research Organisation that is growing rapidly to become a world leader in experimental medicine and digital health technologies for CNS disorders. Due to an increase in demand for theirexpertise, we are looking for a recent graduate who is seeking to develop their skills as a statistical programmer to join their highly skilled scientific team. The successful applicant will support the science team in the conception, delivery, and reviewof statistical analysis, and will be willing to broaden their skill set to support on other scientific activities as required, such as experiment design and manuscript writing.

**Responsibilities**:

- Designing statistical outputs (e.g., tables, figures, and listings).
- Developing statistical analysis plans.
- Programming in statistical tools (mainly SAS).
- Reviewing analysis.
- Developing statistical reports and clinical study reports.
- Presenting data in internal and external meetings.
- Providing ad-hoc statistical support as required.
- Providing support on non-statistical scientific activities as required

Skills and Experience:
Essential
- Recent Bachelor’s degree in a relevant area such as statistics, computer science, biomedical science, experimental psychology, or a related discipline.
- Experience and good knowledge of statistical programming.
- Good understanding of statistical methods, such as linear mixed models.
- Strong conceptual and quantitative skills, for example for choosing statistical techniques and designing visualisations.
- Good communication skills (written and verbal)
- Motivated to learn about and contribute to mental health science.
- Good working knowledge of Microsoft Office.

Desirable
- Experience with programming in SAS preferred, but alternatives also considered would be SPSS, R and Python.
- Experience of data management and/or statistical analysis for clinical trials.
- Understanding of ICH GCP and UK Clinical Trial regulations.

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