Highlights :
- Salary starting at $90,000+
- Manage the whole site team, be a site leader!
- Lead and manage a site from a strategic level
The Company
Our client is a leading site network specializing in clinical trials in a variety of trials in therapeutic areas including vaccines, pediatrics, women's health, rheumatology, respiratory, neurology / psychiatry, and many more! Established in 2006, they now has over 15 research sites all across the US.
They are currently seeking a Site Director to oversee the smooth running of clinical research operations at their Houston location!
The Role
The Site Director 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 / supervision of all research personnel, oversee goal performance, and physical space management.
- Directly oversee site staff and manage staffing needs (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 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
- Manage budget and have an understanding of site financials
Qualifications :
- 5+ years Clinical Research experience at the site level
- 3+ years direct people management experience (with at least 2 direct reports)
- 1+ years experience leading clinical research trials at the Site Manager level or higher
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