Clinical Research Coordinator II
McLaren Medical Group
Non-Health ProfessionalResponsibilities:Assure all study requirements are met and documented and meet both internal and external regulations in accordance with protocol guidelines.Maintain logs, including tracker submissions and update the CTO Oncore database in a timely manner according to CTO SOPs.Design systems for coordinating, compiling and submission of data; design workflow processes and participate in quality assurance measures; coordinate site visits.Manage all patient and/or protocol data as assigned and respond to queries in a timely fashion.Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.Additional Information
Vacancy posted 1 day ago
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