Pre-clinical Study Coordinator

A leading pharmaceutical company in the San Francisco area is in need of a pre-clinical study coordinator. Basic duties include: Designs, plans, implements and coordinates pre-clinical studies according to SOP and GLP (Good Laboratory Practices). These duties include preparation of study protocols, coordination with all necessary departments, ensure proper documentation, assist in finalizing data and preparing study files for archival for in house and contracted studies. Responsible for study planning meetings. Assist in finalization of studies including preparation of reports, figures, appendices and tables including editing/ formatting of various documents. Editing and formatting of various regulatory documents.Required skills: At least intermediate level word processing skills including MSWord and Excel. Excellent verbal and written communication skills. Familiarity with Good Laboratory Practices Guidelines, toxicology and/ or pharmacology in vivo studies. Must be organized and able to handle several tasks/ projects at the same time. Experience with electronic data capture systems is helpful. Science background is a plus.
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. www.shcgpharm.com


REQUIREMENTS
Pharm Group