Beschreibung
Contract Statistical Programmer - Western Germany - 6m Rolling ContractOptimus Life Sciences are working in cooperation with a global pharmaceutical client. We are looking for a senior statistical programmer to join them on a long-term project, being offered as a 6 month rolling contract.
This project will require experience working with FDA Submissions, as well as a strong knowledge of QC and compliance relating to SAS Programming.
If you are interested in applying, please send forward your application to Robert Marrett () and we can organise a call to discuss this position in more detail.
Tasks
- 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
- 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
- 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.
- Proven experience using SAS in the analysis and the reporting of pharmaceutical data
- Working knowledge of database design/structures
Requirements
- Extensive Knowledge of SAS including Base, Macro, Stat, ODS etc.
- Proven experience in Pharmaceutical SAS Programming
- Experience across all Phases of trials and Submissions
- Availability to work on-site in Germany