Duties:
- Program analysis datasets, pooled datasets, tables, listings and figures for Phase I to IV
clinical trials and submission activities
- Perform thorough QC / Validation of own and other programmers work
- Provide input into study protocol, CRF and data structure
- Support senior members of statistical reporting and program / trials statisticians in
maintaining efficient interfaces with internal and external customers
Requirements:
- Strong experience of using SAS in analysis and reporting of pharmaceutical data
- SAS expertise covering Macros, Base & Graph
- Ideally with knowledge of the Oncology therapeutic area (RECIST, CTC grading etc)
Job Types: Full-time, Permanent
Salary: £25,000.00-£35,000.00 per year
Benefits:
Schedule:
- 8 hour shift
- Flexitime
- Monday to Friday
Supplemental pay types:
Ability to commute/relocate:
- Remote: reliably commute or plan to relocate before starting work (required)
Work Location: Remote
Reference ID: LGPSAS2
