Site Manager opportunities in Viera and Maitland, FL!
Highlights :
- $80,000 - $120,000 Salary
- Great benefits including 20 days of PTO and 401k with match
- Lead and manage a site from a hands on and strategic level
The Company
Our client is a fast growing clinical research site network with 18 clinical research sites, some embedded, some stand alone.
Historically, they have focused in vaccine and infectious diseases, but they are now expanding into endocrinology, neurology, and rheumatology studies as they continue to grow! They pride themselves on learning and development for their teams and for high level patient care for their patients!
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
- Directly manage site staff
- 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
Qualifications :
- 3+ years Clinical Research experience at the site level
- 1+ years leadership experience (Sr. CRC and Lead CRCs encourages to apply to get that next step!)
- Willingness to jump in hands on as a CRC as needed
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