Provide study coordinator/data management/regulatory specialist support to the Clinical Trials Office (CTO). This position is onsite in Detroit, Michigan. 

 

 

Responsibilities:

 This position is onsite in Detroit, Michigan. 

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.

·         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

Additional Information Schedule: Full-time Requisition ID: 24004261 Daily Work Times: TBD Hours Per Pay Period: 80 On Call: No Weekends: No