Clinical Research Coordinator

Dayton Physicians Network is looking to add a Clinical Research Coordinator to our team!

Schedule: Monday through Friday 8:00am - 4:30pm

No weekends, evenings or holidays!

Work/life balance schedules

Why work for Dayton Physicians Network?

• Full-time employees are eligible for health, dental and vision benefits
• Company holidays and a flexible holiday!
• Generous Paid Time Off (PTO) Package
• Additional accrual increase after 1 year of service with Dayton Physicians!
• 401K
• Scrub Allotments
• Yearly Bonus Program

Dayton Physicians Network as an Independent Practice

DPN Core Value Expectations

The CARES model reflects the principles that guide our day-to-day behaviors; our decisions, our actions, and our relationships with each other and with the patients and families we serve. All DPN employees are expected to embrace and demonstrate the following:

• COMPASSION: the patient is at the center of all we do
• ACCOUNTABILITY: we hold ourselves accountable for our actions
• RESPECT: we show respect for others
• EXCELLENCE with Innovation: we strive for excellence in all we do
• SERVICE through Collaboration: we provide service to our patients, team members and community.

Essential Duties and Responsibilities

• The clinical research coordinator (CRC) will coordinate and conduct all activities designated by the PI for an assigned clinical trial. The CRC will ensure that the trial maintains accordance with protocols, FDA regulations, GCP/ICH, and IRB requirements.
• Essential Duties and Responsibilities:
• Coordinates trial activities from start up to close out for all assigned trials.
• Prepares, maintains, and coordinates regulatory documents, source documents, trial binders, investigator site files, and all other trial specific regulatory activities for assigned trials.
• Coordinates, conducts, and documents screening and enrollment activities for assigned trials.
• Schedules and leads monitoring visits. Maintains communication with CRO/CRA's.
• Schedules all assigned trial visit needs, obtains protocol specific training, and completes all designated protocol/trial procedures.
• Collects, processes, and manages all data entry for all assigned trials while maintaining accuracy, completeness, and timely submission
• Completes and updates any mailings, billing trackers, trial spreadsheets or other trial specific administrative tasks.
• Processes and ships specimens as required by protocol. Maintains hazardous materials certification.
• Maintains investigational drug inventory, drug accountability records, and other trial inventory/accountability needs.
• Addresses and reports queries, protocol deviations, and participant safety issues and/or adverse events.
• Coordinates with other departments, locations, labs, team members when needed.
• Travels between locations as needed.
• Performs other duties as assigned.

Required Education and/ or Experience

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

General Skill Requirements

• Excellent oral and written communication skills
• Detail oriented and exceptional organizational skills
• Experience working with EMR's, EDC's, Vendor Portals
• Working Knowledge of Microsoft Office (Word, Excel, Outlook, OneDrive, Teams)
• Attendance, punctuality, and flexibility are essential for this role.