Clinical Statistical Programmer

– Technical

• Co-ordinate the creation of analysis dataset specifications
• Co-ordinate the 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

• 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
• Good verbal and written English skills