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Senior SAS Programmer - Oncology
Eingestellt von MSI Recruitment Ltd
Gesuchte Skills: Support, Design
Projektbeschreibung
SENIOR SAS PROGRAMMER - ONCOLOGY
A top 5 pharmaceutical company based Switzerland require a Senior SAS Programmer within Oncology to join their oncology department on a contract basis.
JOB RESPONSIBILITIES:
- 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.
REQUIREMENTS:
- 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)
- Experience within the Oncology Therapeutic area
- Fluent English (Oral & Written).
A top 5 pharmaceutical company based Switzerland require a Senior SAS Programmer within Oncology to join their oncology department on a contract basis.
JOB RESPONSIBILITIES:
- 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.
REQUIREMENTS:
- 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)
- Experience within the Oncology Therapeutic area
- Fluent English (Oral & Written).
Projektdetails
Geforderte Qualifikationen
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Kategorie:
Medien/Design, Sonstiges