Helps monitor study activity to ensures compliance with protocols and with relevant local, federal, and state regulatory and institutional polices.
Helps maintain study records, Including case report forms or regulatory forms
Helps track enrollment status of subjects to documents enrollment and dropouts. Ensures that informed consent is properly obtained and documented
Offers support for quality assurance audits. Identifies protocol problems and assists in problem resolution efforts such as protocol revisions
Helps produce and maintain protocol worksheets, procedural manuals, adverse event reports, institutional review board documents, and progress reports.
Helps with study protocols, evaluates factors such as sample collection processes, data management plans, and potential subject risks. Helps with the development of IRB protocols for sponsored trials and with the interaction with relevant IRB boards
Support the development and execution of research budgets. Helps with the implementation of invoicing systems for clinical trials, orders for supplies, transshipment and more
Helps train the team in scientific and procedural aspects of studies including standards of care, informed consent procedures, or documentation procedures
* Your Virtual CRC works in coordination with your Site Personnel on all tasks assigned under the supervision of your Site Manager.
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