Physicians most often serve as Principal Investigators during clinical phases of the trial and drug development. However, most committed physicians do not have the staff or the time to become involved in the clinical research process. Even when they have the interest, these clinicians are faced with a complex process that includes: making contact with pharmaceutical companies and finding studies relevant to their interest and expertise, accurate and timely completion of large amounts of paperwork, negotiating fees or training their staff to conduct the study which is an expensive and time consuming ordeal. Our highly skilled and knowledgeable staff is available to provide the clinical site with the consultation and expertise on proper trial management and submission of all trial related documents and clarification of issues and query management in a timely manner. The Clinical Research Group can provide on site study coordinators for your research management needs.