Description
A Global Contract Research Organization is reorganizing and growing their Biometrics department. They are hiring by the end of June and positions are contract with a strong expectation of hire. This CRO is known for working on pharmaceutical projects and focuses mostly on phases II and III.This position will involve basic SAS Coding, Managing Macros, writing Macros, validating and performing QC of others code, dataset design - specifically SDTM and ADaM datasets. Candidate may be asked to assist and review specifications to insure they are written to CDISC standards. Programming work will span the entirety of the clinical trial process, including some involvement in the NDA submission processes.
Qualifications:
- 3+ Years Experience with Clinical SAS Programming in the Pharmaceutical, Medical Devices or CRO Industries (Non-Academic Experience).
- Strong Understanding and experience with CDISC Standards.
- Proven Ability with SAS Macros
- Masters Degree Preferred
To find out more about Real please visit www.realstaffing.com