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Job description

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:

• Flexitime
• Work from home

Schedule:

• 8 hour shift
• Flexitime
• Monday to Friday

Supplemental pay types:

• Performance bonus

Ability to commute/relocate:

• Remote: reliably commute or plan to relocate before starting work (required)

Work Location: Remote

Reference ID: LGPSAS2