Clinical Research Coordinator II
Barbara Ann Karmanos Cancer Cn
Detroit, MIFull-time
Behavioral Health Market Context
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Job Description
ncluding 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.
Bachelor's degree required or equivalent combination of education and experience.
Medical and/or science experience/education preferred.
Clinical research certification preferred.
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans
Additional Information
• Schedule: Full-time
• Requisition ID: 26001548
• Daily Work Times: 8am-4:30pm
• Hours Per Pay Period: 80
• On Call: No
• Weekends: No
• 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.
Bachelor's degree required or equivalent combination of education and experience.
Medical and/or science experience/education preferred.
Clinical research certification preferred.
Equal Opportunity Employer of Minorities/Females/Disabled/Veterans
Additional Information
• Schedule: Full-time
• Requisition ID: 26001548
• Daily Work Times: 8am-4:30pm
• Hours Per Pay Period: 80
• On Call: No
• Weekends: No
Qualifications
- •Bachelor's degree required or equivalent combination of education and experience
Benefits
- •Hours Per Pay Period: 80
Responsibilities
- •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
- •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
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