Clinical Research Site Manager

**Manage the clinical site team and site operationsLead and manage a site from a strategic level and help the site become successfulWork with a smaller, but face paced, clinic; Great Teamwork!The RoleThe Site Manager is responsible for directly overseeing the day-to-day clinical operations including planning, organization, and implementation of all aspects of daily clinical research functions. Ensuring optimal conduct of studies, maintaining protocol compliance, meeting clinical data quality standards, optimizing operational flow and continuous monitoring/oversight of clinical trial operations. Also the management and supervision of all research personnel such as overseeing goal performanceDirectly manage site staffManage staffing needs and maintaining staff (interviews, training, performance reviews, etc)Mentor and support direct reports in their responsibilities and functions.Develop and refine subject visit flow and subject binders to ensure on time data capture by properly delegated staff for each subject visitManage and track vital trial metrics and operational objectives for the trial are in conformance to all relevant laws, regulations, GCP guidelines, protocol, and internal SOPs/policies.Study start up, ensure all protocol requirements are met, ordering of proper supplies, development of vendor relationships, coordinate staffing and proper coverageDistribute studies among coordinators, considering the site, coordinator, subject, experience, training & sponsor needs.Participate in the conduct of PSSVs, SIVs and introduce self to all CROs, Project Managers, CRAsProvide back-up for appropriate study tasks, as dictated by patient flow and staff coverageMaintain oversight of accurate and efficient data entry into all systemsAddress all patient, vendor, and sponsor complaintsFacilitate the Quality Control process**5+ years Clinical Research experience at the site level3+ years direct people management experienceStrong leadership and business minded!

Created: 2024-11-01