Clinical Study Coordinator

The Clinical Study Coordinator will be the main point of contact for the clinic, sponsor and Clinical Trials Office for specific protocols.  The qualified candidate will handle regulatory document organization and generation for applicable studies, CRF transcription and query resolution for applicable studies and other protocol-related activities as needed for specific protocols.  Must have the ability to understand and oversee multiple study protocols. Must have knowledge and adherence to Good Clinical Practices (GCPs), including federal and international research guidelines, good organizational skills and knowledge of medical terminology, above average communication skills, particularly in the area of dealing with sponsors and regulatory authorities independently and proficiency in MS Word and MS Excel.  Qualified applicants should submit resumes to hr@jwci.org referencing job code MM/CSC-DM.This institute offers comprehensive and competitive benefits to its employees.  Visit us on the web at www.jwci.org. EOE