ConsignMed, a Niche Clinical Staffing Company since 2003,  and rated by Diversity Business as one of the fastest growing companies in the US  is seeking a The Clinical Research Coordinator will support the In House Trial Program. The CRC is responsible for organizing all aspects of a medical device trial. The duties include: recruiting participants, collecting research data and managing all calendars as they relate to a project. A CRC acts as point person for the clinical-style site, overseeing all operational responsibilities. Position responsibilities: * organize and manager study documentation by distributing, collecting and filing clinical study documents *consent, enroll and follow progress of in house study subjects *train subjects on study protocol and procedures *insert subcutaneous glucose sensors, infusion sets. Other devices as required by the protocol in subjects using GLP and GCP as required by DOPs and SOPs *download clinical study devices and organize computer data files *clean, maintain devices and organize computer data files *manage study inventory including supply ordering and tracking *comply with all training requirements *identify and communicate issues to supervisor in a timely manner *miscellaneous work processing, copying, faxing, mailing or other data management functions as assigned. OTHER QUALIFICATIONS: college graduate, basic use of all Microsoft applications, ability to read, communicate clearly, and basic math skills. *prior experience in clinical research preferred. Basic understand of GCP.