Contract Statistical Programmer
Posted Today by Warman O'Brien
Negotiable
Outside
Remote
United Kingdom
Summary: The role of Contract Statistical Programmer involves supporting various projects for a major pharmaceutical client within a leading European CRO/Consultancy. The position requires a blend of hands-on programming and study lead responsibilities, particularly in Oncology studies. The contract is for 12 months with a strong potential for extension, and it offers a competitive hourly rate. The role is remote or flexible, allowing for work from the UK or Europe.
Key Responsibilities:
- Proven background in Oncology studies
- Comfortable with a blend of hands-on programming and study lead responsibilities
- Strong knowledge of CDISC standards (SDTM, ADaM)
- Proficient in SAS, SQL, STAT, Graph
- Experience with SAPs and process development/improvement
- Exposure across phases I–IV and generating TLFs
- Ability to work independently and drive timelines
- Previous experience within CRO or pharmaceutical environments
Key Skills:
- Experience in Oncology studies
- Hands-on programming skills
- Knowledge of CDISC standards (SDTM, ADaM)
- Proficiency in SAS, SQL, STAT, Graph
- Experience with SAPs and process development/improvement
- Ability to work independently
- Experience in CRO or pharmaceutical environments
Salary (Rate): undetermined
City: undetermined
Country: United Kingdom
Working Arrangements: remote
IR35 Status: outside IR35
Seniority Level: undetermined
Industry: Other
Contract Opportunity – SAS Statistical Programmer (12 Months, Extendable)
Location: UK or Europe (Remote/Flexible)
Industry: CRO / Pharma
Start Date: Feb/March 2026
Contract Length: 12 Months (Strong potential for extension)
Rate: Competitive hourly rate (IR35 would not apply)
A leading European CRO/Consultancy is currently seeking an experienced Contract Statistical Programmer to support a range of projects for a major pharmaceutical client.
Key Responsibilities & Requirements:
- Proven background in Oncology studies
- Comfortable with a blend of hands-on programming and study lead responsibilities
- Strong knowledge of CDISC standards (SDTM, ADaM)
- Proficient in SAS, SQL, STAT, Graph
- Experience with SAPs and process development/improvement
- Exposure across phases I–IV and generating TLFs
- Ability to work independently and drive timelines
- Previous experience within CRO or pharmaceutical environments
This is a great opportunity to work on high-impact studies in a collaborative environment with a respected name in the industry.
Interested? Apply now to learn more and discuss next steps.