Contract Statistical R and SAS Programmer
Posted 3 days ago by Warman O'Brien
Negotiable
Undetermined
Undetermined
Twickenham, England, United Kingdom
Summary: The role involves joining a global pharmaceutical organization as a Statistical Programmer on a contract basis for 12 months. The position focuses on providing statistical programming support for clinical trial analysis and reporting, collaborating with statisticians and cross-functional teams. The candidate will be responsible for developing datasets and ensuring compliance with programming standards and regulatory requirements.
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
Key Skills:
- 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
Salary (Rate): undetermined
City: Twickenham
Country: United Kingdom
Working Arrangements: undetermined
IR35 Status: undetermined
Seniority Level: undetermined
Industry: Other
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