CRS II PH 45931/62704

CRS II needed to assist clinical trial leader or may act as clinical trial leader in the management of individual clinical trials. Under the direction of the clinical trial leader or clinical research manager, conducts day-to-day activities including protocol writing, trial administration, report writing and interaction s with other line units in support of clinical trials. Contributes to continuous improvement of process, Contributes in preparing clinical trial protocol summaries and clinical trial protocols. Contributes in preparation and implementation of project specific training programs and training materials for internal and external staff. Contributes in monitoring safety, eligibility, enrollment and data consistency. Contributes in preparing draft clinical trial reports and draft summaries. 1-3 Years Experience.

Smith Hanley Consulting Group,a division of Smith Hanley, specializes in providing clinical trials staffing to national pharmaceutical companies offering long-term contract services of Statisticians, SAS Programmers, Data Managers, Clinical Research Associates and other clinical specialties. Our professional recruiters are recognized leaders in the industry by placing junior to senior candidates into rewarding positions within leading pharmaceutical companies throughout the United States. For more than twenty years, we have built extensive client relationships. We strive to help our candidates make decisions that are consistent with their professional values, priorities and goals as well as provide our clients with candidates that meet their employment needs.