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Principal Statistical Programmer
| Category | Statistics & SAS |
|---|---|
| Job Ref | LC/HQ00014715 |
| Job Type | Permanent |
| Salary | Excellent salary |
| Location | Switzerland - Basel |
25 Aug 2010
A leading pharmaceutical company currently has urgent requirements for 4 permanent Principal Statistical Programmer. You would be based in there HQ in Switzerland.
KEY RESPONSIBILITIES
- Coordinate programming activities across several trials and indications with a given compound including publication and regulatory submission activities.
- Lead the indication/project team including resources planning and coordination of the different programming sites (Basel, India, Japan and US)
- Make certain that indication/project documents and specifications are consistent and comply with company standards by providing input into Study protocol, CRF and Data structures and outputs (listings, tables and figures) for phase I-IV clinical trials and 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.
- Support quality control and quality audit of deliverables.
- Participate as required at all meetings, discussions and activities covering aspects of Statistical Reporting on trial/project level activities.
- Track clinical trial milestones for statistical reporting deliverables.
- Maintain records for all assigned projects and archiving of indication/project analysis and associated documentation.
- Maintain efficient interfaces with internal and external customers and communicate effectively across line functions.
- Program according to specifications, analysis datasets, pooled datasets, listings, tables and figures for phase I-IV clinical trials and for SCS and SCE with high quality and within milestones.
Minimum requirements
- Ideally a Bachelor/Master's degree in Mathematics, Statistics, Data Analysis Program or Computer Science (or equivalent degree with experience).
- Ability to lead and coordinate programming work across several studies.
- Solid experience using SAS in the analysis and the reporting of pharmaceutical data
- Working knowledge and expertise with SAS (including SAS macro language)
- Strong analytical skills and the ability to think laterally
- Working knowledge of database design/structures
- Good understanding of global clinical trial practices, procedures and methodologies.
- Good understanding of regulatory requirements (e.g. GCP, ICH)
- Fluent English (oral and written)
For further information please contact
Laura Christie
Email: laura.christie@hayspharma.com
Services advertised by Hays Pharma are those of an Agency and/or an Employment Business
