Clinical Research Coordinator/Study Coordinator/Study Associate
 We are looking for a mature, non-smoking person with extensive prior medical research experience who is CCRC certified by the ACRP or CCRP certified by SoCRA. Especially if your experience was in internal medicine as we do primary care drug studies usually involving: HTN, DM, Cholesterol, Osteoporosis and Obesity.
 You would report to our director of clinical research. The duties would include: meeting and greeting the research subject volunteers, do their vital signs, record their current medications, AEs, SAEs, and list their chief complaints. In addition, to be able to draw blood, perform EKGs, and provide the patient with initial informed consent. You will need to obtain the proper information from the patients to fill out the case report forms properly, and interact with the clinical research associates/monitors from the sponsor drug companies to ensure their protocols are followed.
 Salary is commensurate with prior experience. Please fax your CV/resume in confidence to 561-745-8982.