Clinical Research Coordinator – Oncology Trials & Benefits

Dayton Physicians, LLC; Kettering (OH); On-site; USD 60,000 - 90,000; Full time

Job summary

Dayton Physicians Network in Ohio is seeking a Clinical Research Coordinator to join our team and oversee trial activities from start-up to close-out.

The CRC will manage regulatory documents, enroll participants, coordinate visits, monitor safety, and collaborate with departments across locations. A health, dental and vision benefits package and generous PTO are offered, with occasional travel between sites. Experience with EMR/EDC systems and strong communication skills are preferred.

Qualifications

• Bachelor's degree in nursing or health-related field preferred.
• Oncology/Hematology/Urology/Radiation Oncology clinical research experience preferred.
• Familiarity with Good Clinical Practice (GCP) and Institutional Review Board (IRB) requirements.

Responsibilities

• Coordinate and conduct all activities designated by the PI for an assigned clinical trial.
• Coordinates trial start-up to close-out for all assigned trials.
• Prepare, maintain, and coordinate regulatory documents, source documents, trial binders, investigator site files, and other trial-specific regulatory activities.
• Coordinate screening and enrollment activities for assigned trials.
• Schedule and lead monitoring visits; maintain communication with CRO/CRA's.
• Schedule trial visits, obtain protocol-specific training, and complete all designated procedures.
• Collect, process, and manage data entry for all assigned trials with accuracy and timeliness.
• Update mailings, billing trackers, and trial spreadsheets.
• Process and ship specimens; maintain hazardous materials certification.
• Maintain investigational drug inventory and accountability records.
• Address queries, protocol deviations, and participant safety issues.
• Coordinate with other departments and travel between locations as needed.
• Perform other duties as assigned.

Skills

Excellent communication

Detail oriented

EMR/EDC experience

Microsoft Office

Punctuality & reliability

Education

Bachelor's degree in nursing or health field

Oncology/Hematology/Urology/Radiation Oncology clinical research experience

Tools

EMR systems

EDC systems

Vendor Portals

Microsoft Office

Job description

Dayton Physicians Network in Ohio is seeking a Clinical Research Coordinator to join our team and oversee trial activities from start-up to close-out.

The CRC will manage regulatory documents, enroll participants, coordinate visits, monitor safety, and collaborate with departments across locations. A health, dental and vision benefits package and generous PTO are offered, with occasional travel between sites. Experience with EMR/EDC systems and strong communication skills are preferred.