Beschreibung
Main 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.
Experience
- 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)
Start dates are available immediately, initial contacts will be 9 months with the potential for further extension. Please apply with a recent CV to be considered