Strategic Program Coordinator for Clinical Trials

The Ohio State University Wexner Medical Center; Columbus (OH); On-site; USD 45,000 - 55,000; Full time

Job summary

A prominent medical center in Ohio is seeking a Program Coordinator for the Clinical Trials Office. This entry-level position will involve coordinating activities related to NCI contracts, overseeing data submissions for various research groups, and ensuring compliance with grant requirements. The ideal candidate will hold a Bachelor's degree and have at least one year of relevant experience. Join a team dedicated to advancing cancer research and ensure the accuracy and timeliness of research data submissions.

Qualifications

• One year of relevant experience required.

Responsibilities

• Coordinate activities of NCI contracts in the Clinical Trials Office.
• Oversee data submission timelines for disease team groups.
• Track and supervise data collection activities.
• Ensure timely data submissions and compliance with grant requirements.
• Lead maintenance of NCI roster and registrations for CCC investigators.
• Participate in conference calls and meetings for compliance.
• Coordinate weekly Phase 1 meeting speakers schedule.
• Record and distribute meeting minutes appropriately.
• Work closely with external academic institutions and their research teams.
• Identify training needs of the research staff regarding LAPS and UM1.
• Participate in NCI audits and manage scheduling.
• Monitor clinical trials to ensure they are up to date.
• Develop regular progress reports for the Project Manager.
• Maintain group calendar and group email inbox.

Education

Bachelor's degree or equivalent experience

Job description

A prominent medical center in Ohio is seeking a Program Coordinator for the Clinical Trials Office. This entry-level position will involve coordinating activities related to NCI contracts, overseeing data submissions for various research groups, and ensuring compliance with grant requirements. The ideal candidate will hold a Bachelor's degree and have at least one year of relevant experience. Join a team dedicated to advancing cancer research and ensure the accuracy and timeliness of research data submissions.