Description
Contract Statistical ProgrammerCopenhagen
4-6 Month Contract
€75/hr
Optimus Life Sciences are working with a global pharmaceutical consultancy based in Denmark. We are looking for a freelance SAS Programmer to work on CDISC SAS programming work (SDTM/ADAM), structuring data sets and reproducing tables.
This project will require experience working with FDA Submissions, as well as a strong knowledge of QC and compliance relating to SAS Programming, specifically TLFs. CDISC knowledge is important to this role, experience with ADaM Datasets is a must have for the client.
The position will be based between 2 clients, requiring 3 days per week working on site for one client and flexible working for the other 2 days - this is to be discussed with the hiring manager. Interviews can take place as soon as possible.
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
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.