Description
Contract SAS Programmer - East Coast US - 12m ContractOptimus Life Sciences are working with a well-known international pharmaceutical client to locate an on-site worker for a 12-month contract. The role will be a to join them urgently on a long-term project on-site in the USA. This role will focus on programming in relation to an FDA submission, oncology experience would be preferable.
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 FDA Submissions
- Availability to work on-site in the USA
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.