Clinical Trial Manager - 98102

In order to be considered for a position, candidates must be located in one of the following five states: CA, MA, NC, OR, or WA.

• Manages, provides guidance and oversight for all components of a clinical trial from protocol development through clinical study report
• Develops and contributes to development of study plans and manuals
• Manages CRO, including overseeing clinical monitoring, investigational selection and site management
• Responsible for oversight of Trial Master File (TMF) for inspection readiness.
• Helps develop and manage clinical budgets and contracts plans for clinical trials.
• Responsible for managing overall study budget, including review of vendor invoices for accuracy.
• Collaborates with CRO and investigational sites, as needed, to complete and execute trial deliverables as required per protocol and contract.
• Responsible for creating and maintaining timelines for a clinical trial, including study start-up, enrollment projections, study conduct, and close-out activities with project goals, and using these timelines to track and manage a trial’s progress