Provide study coordinator/data

management/regulatory specialist support to the Clinical Trials Office (CTO).

Responsibilities:

• Assure all studyrequirements are documented and meet both internal and externalregulations in accordance with protocol guidelines.

• Maintain logs,including tracker submissions and update the CTO Oncore database in atimely manner according to CTO SOPs.

• Respond to queriesin a timely fashion.

• Schedule andparticipate in monitoring visits and participate in multidisciplinary teamprogram meetings as required.

• Assistmultidisciplinary 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