We are looking for a Site Manager who is eager to step in and make an immediate impact. The Site Manager provides on-site, daily leadership with the execution and coordination of clinical research activities according to SOPs, FDA and ICH/GCP guidelines. The SM will provide direction for growth and development of this expanding research site. Responsibilities: *lead, select, counsel and develop all site staff to ensure they display necessary knowledge and skills to achieve objectives; *plan and organize the site to optimally meet client needs. Analyze collected data to identify patterns and trends for opportunities to improve client care and service performance; *foster communication internally as well as with other AMR sites; *direct and guide staff on study specific tasks. Assist in training staff; *serve as study coordinator for trials as dictated by the site’s needs; *interact with community, staff, monitors, PI and site owners;
5 yrs as a CRC; Management training and experience is essential; RN/LPN a plus; Exceptional organizational skills, Attention to detail and follow through; Must be strong leader, set the example and train others; Must be professional, possess a high degree of urgency and self-motivation and have strong work ethic.
Internal Number: CRCM
About AMR - (New Orleans Center for Clinical Research)
NOCCR is a dedicated research facility conducting clinical trials across all phases of research. Established in New Orleans, LA in 1985, NOCCR still maintains the original Canal Street location, but also has additional offices. Following Hurricane Katrina, the Phase I unit and company headquarters were moved to Knoxville, TN. NOCCR Knoxville and Volunteer Research Group (VRG) are headquartered inside East Tennessee’s premier research hospital.