RESPONSIBILITIES INCLUDE: - maintain administrative systems (tracking and other) for clinical projects according to Covance SOPs. - assume a coordinating role for the project team concerning administrative matters. - provide clerical support to project team (e.g. word processing, proofreading and editing correspondence, large and small documents, mailings, shipment of study files, fax and photocopy documents, assemble study documents, and arrange meetings, etc.) . - provide telephone coverage and related support duties. - set up and maintain clinical investigator files and documentation. - prepare investigator budget payments and tracking systems; generate tracking reports as assigned. - do data entry and maintenance of selected study tracking databases. - prepare monitoring visit documentation for Clinical Research Assistants and above, as requested by supervisor. - prepare study-related documents and other materials for delivery to archives, at appropriate intervals. - perform other administrative duties as assigned by management.