For our client, a healthcare company in Basel, we are seeking for a
SAS Programmer
Your job responsibilities
- Program according to specifications, analysis datasets, listings, tables and
figures for phase 3 studies
- 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, CRF 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
Requirement
- 5 years (preferably 8 years) 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)
- Knowledge of Cardiovascular / Metabolism TA
- Good team player
- Good organizational
- Continuous improvement mentality and attention to detail
- Fluent English (oral and written)
Contact
- [log in to unmask], +41'61'560'77'28
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