Description
The Clinical Data Programmer is responsible for both EDC and Report (listings) Programming on assigned studies. This is conducted by performing system setup and testing following standard process procedure and SOP.Ensures clinical study databases are integration ready
- Some knowledge of ICH, FDA, and GCP regulations and guidelines; Knowledge of CDASH, SDTM and CDISC
- SQL or SAS programming skills preferred
- EDC Systems; Medidata Rave and Lab Admin experienced preferred
- Reporting tools; JReview, BOXI
- Good project management skills with the ability to multitask
Requires some supervision and guidance on determining methods and procedures on new assignments.
IDEAL CANDIDATE: 2-5 years of Clinical Programming experience. Oncology preferred.
To find out more about Real please visit www.realstaffing.com