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Senior SAS Programmer
Eingestellt von Michael Bailey Associates - Munich
Gesuchte Skills: Support, Design
Projektbeschreibung
Senior SAS Programmer (Oncology)
+ 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.
+Program Programmer
+Local Head SR
+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 in Oncology therapeutic area
+Good team player
+Good organizational
+Continuous improvement mentality and attention to detail
+Fluent English (oral and written)
Frank Arnold
Pharmaceutical Recruitment ConsultantMichael Bailey International is acting as an Employment Business in relation to this vacancy.
+ 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.
+Program Programmer
+Local Head SR
+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 in Oncology therapeutic area
+Good team player
+Good organizational
+Continuous improvement mentality and attention to detail
+Fluent English (oral and written)
Frank Arnold
Pharmaceutical Recruitment ConsultantMichael Bailey International is acting as an Employment Business in relation to this vacancy.
Projektdetails
Geforderte Qualifikationen
-
Kategorie:
Medien/Design, Sonstiges