Description
Rated #1 Biopharma in the world, this reputable company in New Jersey seeks a Senior Statistical Programmer to join their growing group! This opportunity is a support/lead role working on mass complex studies in Phase II - III clinical trials.The role is:
Senior Statistical Programmer
- Office based
- ISS/ISE NDA submissions
- Report into the AD of Statistics
- Work very closely with the statistician
- Therapeutic areas covered: CV, Oncology, Translational medicine
All potentital candidates must meet the following requirements to be considered:
- A minimum of 4 + years clinical trial experience
- CDISC knowledge
- Good communication skills
- Masters is preferred
- GC or US citizen
If this opportunity is of interest to you feel free to submit your resume directly, and reach out to Allison Idarraga at for further details. Other opportunities are open at various levels so feel free to inquire for details!
To find out more about Real please visit www.realstaffing.com