Clinical Research Coordinator II
McLaren Medical Group
Non-Health Professional
Responsibilities:
- 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 4 days ago
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