Job Information
McLaren Health Care Clinical Research Coord I in Detroit, Michigan
Description
Job Summary: Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO).
Responsibilities:
Assure all study requirements are 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.
Respond to queries in a timely fashion.
Schedule and participate in monitoring visits and participate in multidisciplinary team program meetings as required.
Assist multidisciplinary team in research activities.
Qualifications
Qualifications:
Bachelor’s degree required or equivalent combination of education and experience.
Medical and/or science experience/education preferred.
Proficient with the Microsoft suite including Excel and Power point.
Demonstrated attention to detail.
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans
Job: Non-Health Professional
Primary Location: Michigan-Detroit-Mid Med Building
Organization KCI30-Karmanos Cancer Institute
Employee Status Regular
Shift Day Job
Job Type Standard
Schedule Full-time
Req ID: 20009191