Job Information
McLaren Health Care Clinical Research Coordinator II - McLaren Careers in Detroit, Michigan
Job Summary:
Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena.
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.
Job Summary:
Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). Manage independent assignment, providing excellent customer support and guidance in the clinical trials arena.
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.