Full-time opportunity for a Research Coordinator (Study Coordinator focus). This is a dual role position with most time dedicated to study coordination duties and some time dedicated to administrative duties. Coordinator screens potential participants for entry into clinical trials, provides support in coordinating all aspects of the clinical management of research participants according to clinical trial protocols. Maintains regulatory documents, completes case report forms and participates in activities of monitoring/auditing as assigned by the Director of Research. 

Bachelor's degree in nursing preferred or a bachelor's degree in a healthcare field or equivalent healthcare experience preferred. These qualifications may be waived if applicant has prior experience in clinical research or healthcare field. Must be proficient in keyboarding for data entry and letter writing and proficient in Microsoft Office applications including Word, Excel and Access. This position requires an aptitude for numbers and a meticulous approach to detail. Excellent interpersonal skills are required.