Director of Regulatory Affairs
 We are looking for a mature, non-smoking person with extensive prior medical regulatory affairs research experience who is RAC certified by RAPS. Especially if your experience was in internal medicine as we do primary care type 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, provide the patient with initial informed consent, obtain the proper information from the patients to help the CRC fill out the case report forms properly, interact with the clinical research associates/monitors from the sponsor drug companies to ensure their protocols are followed properly, and to maintain the regulatory affairs binders up to date. In addition, to negotiate budgets, arrange advertising for the drug studies, and monitor the progress of and adjust the advertising accordingly to maximize patient recruitment.
 Salary is commensurate with prior experience. Please fax your CV/resume in confidence to 561-745-8982.