Design and manage all aspects of clinical data management, statistical programming, and reporting of clinical data deliverables. Develop study timelines and CTMS. Build and run custom queries using Business Objects to retrieve data from the database. Set up, maintain, and close the local Trial Master File (eTMF) and Investigator Site File for Good Clinical Practice compliance. Master’s degree in Science, Public Health, Healthcare Administration, Biology or Technology (any) is required. Work location: South Plainfield, NJ and various unanticipated locations throughout the U.S.Send Resume to HR Dept., Unicon Sciences, Inc., 51 Cragwood Road, Suite 106, South Plainfield, NJ 07080.