Document Management Coordinator

Document Management Coordinator needed in Stamford, Connecticut.

Compensation is commensurate with experience.

Assist department with QAing/scanning/uploading clinical research study documents into validated system that is compliant with ICH/GCP/FDA guidelines and Company policies and Standard Operating Procedures and Regulatory Document Management processes.

The selected candidate for this position will be responsible for assisting RDM with QA, scanning and/or uploading documents associated with closing out studies and additional clinical relative documentation in need of being uploaded to DMS. Additionally this person may support the processing efforts of submissions to the FDA including but not limited to hyper linking text within large documents. This person should have the following qualities and most importantly attention to detail, able to follow direction, high quality work standard, familiarity with clinical trial documentation and diligence.
REQUIREMENTS
see job description