Our client is looking for an SAS Programmer to join their Swiss team on a contract basis.
Working as an SAS Programmer, your main responsibilities will include:
- Coordinate programming activities across several trials with a given compound including publication and regulatory submission activities.
- Develop programming specifications for analysis datasets, pooled datasets and deliverables in consultation with the statistician.
- Develop and comply with project/study programming standards and specifications following internal guidelines
- Program according to specifications, analysis datasets, pooled datasets, listings, and figures for clinical trials and submission activities
- Support quality control and quality audit of deliverables
- Provide input as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial level activities
- Track clinical trial milestones for statistical reporting deliverables.
- Maintain records for all assigned projects and archiving of trial/project analysis and associated documentation.
- Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.
How to Apply
Please contact Jonathan Hart-Smith at CK Clinical for more details or to apply for this position on +44 (0)1438 743047 or email email@example.com
About CK Clinical
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