Description
Under supervision of the heads of statistical programming group, you will have the responsibility for all programming aspects of the international clinical trials you are assigned to. Evolution to international project programming level can be foreseen in the future depending on candidate capacities and progression.
Your main responsibilities as a senior trial programmer will be:
- Contributing with the trial statistician to the writing of the TSAP technical specifications: derived dataset structure and content, layout of Tables, listings and figures as well as any other specifications needed for optimized follow up of the trials.
- Programming in SAS V9 all programs generating the derived datasets sets, tables, listings and figures as per specifications and according to the quality and time allocated.
- Be responsible for checking the quality of your own work and documentation attached to its traceability.
- Attend meetings, discussions and activities related to the production of all deliverables for the clinical trial report.
You will have many contacts, interactions and discussions with project team being at national or international level. Good spoken and written English is mandatory. A minimum knowledge of clinical trials terms and usage is required.
You should have very good relationship skills and can also work independently.
SAS skills: SAS Base, SAS SQL and SAS Graph. SAS stat knowledge is a plus.
Minimum experience required within Pharma or CRO: 5 years