Statistical Programmer
Warman O'Brien
Warrington, United Kingdom
4 days ago
Role details
Contract type
Temporary to permanent Employment type
Part-time / full-time Working hours
Regular working hours Languages
English Experience level
Senior Compensation
£ 70KJob location
Remote
Warrington, United Kingdom
Tech stack
Clinical Data Repository
Data Integrity
Data Structures
SAS (Software)
Information Technology
Job description
- You'll lead statistical programming projects, ensuring high-quality, on-time deliverables.
- This includes developing and validating SDTM and ADaM datasets, performing QC reviews, and ensuring CDISC compliance.
- You'll resolve Pinnacle 21 validation issues, review TLFs for consistency, and contribute to regulatory submissions.
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Requirements
- A Master's or Ph.D. degree in Statistics, Biostatistics or Computer Sciences.
- At least 6 years' experience in clinical trial Statistical Programming.
- Excellent knowledge of SAS essential with R advantageous.
- Good working knowledge of data structures e.g. CDISC, SDTM, ADaM,
- Comprehension of clinical data standards (CDISC), TLFs, and submission guidelines.
Benefits & conditions
What in it for you:
- The opportunity to be involved in a growing organisation.
- Focus on career development and progression.
- Enjoy a healthy work-life balance with flexible hours that fit your lifestyle.
- Fully remote in the UK
- Generous remuneration package.
What to do next
About the company
Join a fast-growing, independent CRO providing a broad range of expertise-based clinical research services to worldwide pharmaceutical, biotechnology, and medical device industries.
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