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