Clinical Study Coordinator

CLINICAL STUDY COORDINATOR JOB DESCRIPTION:  The qualified candidate will be responsible for:  -tracking documents including site contracts, confidentiality and investigator agreements, vendor contracts, CRFs, regulatory documentation, and other study documentation -coordinating the payment of clinical sites and vendors with the accounting department -Coordinating regulatory document collection -Creates clinical files and maintains documents in clinical files  -Assists in production of study specific documentation including correspondence, clinical study forms, site investigator binders,  -Prepares and processes documentation for clinical supply shipment and accountability -Tracks patient enrollment and reviews progress of data entry into electronic Case Report Forms  -Assists with reviewing and tracking of monitoring visit reports  -Manages the administrative needs of the groups including courier shipments, photocopying, telephone coverage, organization of meetings and teleconferences, generation of meeting minutes  -Facilitates resolution of study related issues through communication with site personnel, clinical trial vendors including central laboratories, monitoring CROs, etc.  -Works with internal departments such as finance/accounting, regulatory affairs, and quality assurance to ensure completion of clinical operations activities JOB REQUIREMENTS:  2+ years experience PC and MS Office skills required this position requires verbal and written communication, organizational, presentation and interpersonal skills  *CLIENT OFFERS EXCELLENT BENEFIT PACKAGE*