Description
-Professional Summary- Fourteen years of experience working with Contract Research Organizations (CROs), expertly gathering and analyzing data for highly confidential clinical trials. Excellent knowledge in clinical research regulatory requirements, study protocols, FDA, good Clinical Practices, 21 CRF Part 11, HIPPA, CDISC, ICH guidelines and Standard Operating Procedures. Proficient skills in Electronic Data Capture (EDC) systems (Rave, Inform, CTMS) and Electronic Data Master File. Proven desire for achievement and continued professional growth.
Work Experience
| COMPANY | POSITION HELD | DATES WORKED |
|---|---|---|
| Covance Clinical Development Services | Document Specialist Clinical Data Associate Ii | 3/2017 - 9/2017 |
| River Front Llc | Data Coordinator | 7/2015 - 3/2016 |
| Xerox | Benefits Associate | 1/2013 - 7/2015 |
| Pharma Net (Inventiv) | Data Analyst Senior Quality Control Associate Senior Data Entry Associate | 8/2009 - 9/2012 |
| Theradex | Data Entry Technician | 6/1994 - 6/1999 |
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