Clinical Documentation Specialist
Integrated Resources, Inc ( IRI )Massachusetts, United States
Posted July 29, 2015
Full Time
About the Company
A premier staffing firm recognized as one of the tri-states most well-respected professional specialty firms.
Job Description
Clinical Documentation Specialist at Integrated Resources, Inc. responsible for QC Review, coding, verification, and document tracking. Must have TMF Document experience and 2+ years of experience in Pharma/Bio.
Requirements
- QC Review of pre-study and study documents
- Coding of administrative and regulatory documents
- Verification of documentation, maintenance of document tracking system
- Collaborating with CTM to determine to issues in regulatory documentation