Position Overview & Specifications

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