Clinical Study Manager

Smith Hanley is currently seeking a Clinical Study Manager for the Delaware area.Successful candidate will assume site management activities for a Phase III trial. Specific tasks may include managing sites, reviewing reg docs, reviewing consent forms, writing protocols, designing CRFs, reviewing monitoring reports, negotiating CSA, tracking document flows, updating IMPACT, working with DSRI, working with study team on process flows and communication plans, overseeing grant and payment process, working with AZ regional monitoring group, and managing an academic research organization. Position will also include data management activities which may include working with web based data capture system, reviewing and validating data, writing data queries, reviewing data tables and listing.Experience/Min Requirements: 2 years experienceEducation/Degree: BA/BS degree required, preferably in science fieldInterested candidates should send resumes to Chris Nordhorn @ [Click here for email] or phone at 800-684-9921 x278Smith 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