We are supporting a global pharmaceutical organisation in the search for an experienced Statistical Programmer to join a specialist biometrics function on a contract basis for 12 months initially.
This role will focus on supporting independent statistical and safety analysis activities across clinical development programmes, working closely with statisticians and cross-functional study teams.
Key Responsibilities
- Deliver statistical programming support for clinical trial analysis and reporting activities
- Develop and validate datasets, tables, listings, and figures (TLFs)
- Support independent safety and statistical analysis workstreams
- Collaborate with biostatistics and clinical teams to ensure high-quality deliverables
- Contribute to programming standards, QC processes, and regulatory compliance activities
Required Experience
- Strong hands-on experience with SAS programming
- Experience using R within a clinical research or pharmaceutical environment
- Background in statistics, biostatistics, or statistical programming
- Experience supporting clinical trial analysis within biotech/pharma/CRO settings
- Understanding of clinical data standards and reporting requirements
Desirable
- Experience supporting safety analyses or independent statistical review activities
- Familiarity with regulatory submission environments
- Previous experience working within global clinical development teams