Clinical SAS Statistical Programmer required for a brand new role at an expanding and ambitious clinical research organization based in New Jersey.
My client, easily commutable from New York, is aiming to double in size over the course of the next two years which will give you huge opportunities if you join now!
This is a fantastic new SAS opportunity to join a growing biostatistics team where you will be expected to utilize your experience in SAS, while handling and resolving all database and programming issues. This will involve providing a leadership role in statistical programming and reporting areas as well as performing database set ups and database validation.
In this role you will develop SAS programming codes and test SAS codes for clinical trial database checks. You will archive clinical trial data and program information in accordance to SOPs and guidelines. You will also design statistical analysis dataset modules and create complete, efficient analysis datasets.
The ideal candidate for this global role will have a good understanding of Clinical Data alongside solid SAS programming experience within a pharmaceutical/CRO environment. You should have at least 6 years relevant clinical trial statistical programming experience and should be at least BSc educated in statistics, math, computer science or another science related discipline.
On offer is a generous salary and benefits scheme including plus good opportunities for development.
This job was posted 30+ days ago, and has expired.