Co-ordinatethe creation of analysis dataset specifications
Co-ordinatethe programming of analysis datasets, using specific SAS macros.
Co-ordinate the production of tables, listings & figures
Quality Control of project deliverables
Set & maintain professional programming standards
Maintain & archive program documentation - both electronic & paper - in an appropriate manner
Maintain professional programming standards
Profile
BSc, MSc or equivalent by working experience
2 to 5 years of relevant clinical trial SAS experience preferably in a similar role
Proficient SAS programming skills with mastery of SAS/STAT SAS/BASE, SAS Studio, SAS macro language. SAS/GRAPH is a nice to have.
Capacity to interface with clinicians, statisticians and data managers as statistical programmer in charge of a clinical trial.
Good knowledge of statistical approaches applied in cancer clinical trials with a focus on survival analysis techniques.
Capacity to work independently or under the guidance of a senior programmer.
Knowledge and practice of CDISC SDTM and ADaM data standards.
Ability to work complying to the company programming SOPs, data standards and macro library as well as capacity to develop project specific code independently under company SOPs.
Ability to effectively manage time and prioritize project work
Good organization skills
Creative and innovative, able to adapt to dynamic environment
