Highlights:
- 6 month contract
- Competitive hourly pay and benefits if needed!
- Manage the 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 contract 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. This site is embedded so there are not other research staff, you will be managing the clinical research aspects alongside the PI.
- Comfortable being the only CRC at the site (There is a PI and support staff for the office, not NOT other research staff)
- Manage patient recruitment, consent, screening, and visits
- 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
- Ensure all protocol requirements are met, ordering of proper supplies
- Participate in the conduct of PSSVs, SIVs and work with all CROs, Project Managers, CRAs
Qualifications:
- 3+ years Clinical Research experience at the site level
- Willingness to handle all CRC tasks in a solo environment
- Ability to work on side daily in Burke, VA for 6 months
