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Trial Master File/Document Quality Coordinator
I am a Document Quality Coordinator/Clinical Trial Assistant with 3 years experience with pharmaceuticals and 3 years with CROs. My expertise in with organizing, maintaining, and quaity checking Investigator files and General files, hard copies and electronic documentation. I keep track of updates on essential documents from sites - IRB approvals, CVs, Medical licenses, and Financial disclosures,protocol, IB, study manual signature pages.
Agricultural Technician
About Me
Industry: |
Science & Biotech |
|---|---|
Occupation: |
Agricultural Technician |
Education level: |
Bachelor |
Will Relocate: |
Yes |
