What are the responsibilities and job description for the Clinical Research Site Manager position at SQRL?
Highlights :
80,000 - $110,000 based on exp benefits
Manage the clinical site team and site operations
Lead and manage a site from a hands on and strategic level
Work with a great, already established team and site!
The Role
The 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 performance
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 visit
Manage 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 coverage
Distribute 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, CRAs
Provide back-up for appropriate study tasks, as dictated by patient flow and staff coverage
Maintain oversight of accurate and efficient data entry into all systems
Address all patient, vendor, and sponsor complaints
Facilitate the Quality Control process
Qualifications :
3 years Clinical Research experience at the site level
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