At a Glance
- Tasks: Support clinical development by designing and analysing clinical trials from start to finish.
- Company: Join a leading organisation in the clinical research field.
- Benefits: Competitive pay, flexible working arrangements, and opportunities for professional growth.
- Other info: Collaborative environment with a focus on innovation and quality.
- Why this job: Make a real difference in healthcare by contributing to vital clinical trials.
- Qualifications: Extensive experience in clinical trial statistics and proficiency in SAS or R.
The predicted salary is between 63000 - 77000 £ per year.
Contract Statistician
We are seeking an experienced Contract Statistician to support clinical development from early to late-stage development.
The successful candidate will need to have extensive experience in the statistical design, analysis, and reporting of clinical trials across Phases I–III, with a strong understanding of regulatory requirements and submission standards.
Key Requirements
- Proven experience in statistical design and analysis of Phase I–III clinical trials.
- Expertise in developing statistical analysis plans (SAPs), protocol input, sample size calculations, and study design.
- Hands-on experience supporting regulatory submissions (e. g. FDA, EMA), including preparation and review of submission-ready statistical documentation.
- Proficiency in SAS and/or R for statistical programming and analysis.
- Strong knowledge of ICH guidelines, CDISC standards (SDTM/ADa M), and Good Clinical Practice (GCP).
- Excellent communication skills and the ability to work effectively within multidisciplinary project teams.
This is a contract opportunity for a highly motivated statistician who can provide expert statistical leadership and deliver high-quality outputs within project timelines.
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