Statistical (SAS) Programmer

CONTRACT: 2 x SAS Programmer
Phase I Oncology
6 month rolling contract

Accountabilities/Responsibilities:

Support quality control and quality audit of deliverables
Develop and comply with project/study programming standards and specifications following internal guidelines
Provide input into study protocol, CFR and data structure
Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities
Support senior members of statistical reporting and program/trial statisticians in maintaining efficient interfaces with internal and external customers

Essential Skills & Capabilities:

Experience using SAS in the analysis and the reporting of pharmaceutical data
Working knowledge of database design/structures
Expertise with SAS (including SAS macro language)

Desirable Skills & Capabilities:

Experience on Phase I studies and/or PK data
Experience in Oncology therapeutic area

Pharmaceutical, clinical trials, SAS programming, statistical programming, statistics, oncology