Clinical Trials Coordinator - Oncology Research

Tennessee Oncology; Nashville (TN); On-site; USD 60,000 - 75,000; Full time

Job summary

Tennessee Oncology is a community-based cancer care network founded in Nashville, focusing on access to high-quality care and research. This Clinical Trial Specialist I role supports the research team to ensure rigorous adherence to GCP/ICH guidelines while mentoring by more senior staff.

The position involves managing day-to-day trial activities, coordinating with cross-functional teams, and maintaining essential trial documentation to support compliant and efficient studies.

Qualifications

• Bachelor’s degree or equivalent; 1 year clinical trials experience required.
• Knowledge of GCP/ICH guidelines is preferred.
• Proficient with Microsoft Office (Word, Excel, PowerPoint).

Responsibilities

• Manage day-to-day operations of Phase I–IV protocols per GCP/ICH.
• Lead cross-functional study teams and liaise with vendors.
• Verify patient eligibility and monitor trial timelines.
• Attend Site Initiation, monitoring, and closeout visits.
• Maintain informed consent records and essential trial documents.
• Provide updates to study team and sponsor.

Skills

Multitasking

Clinical trial protocols

Communication

Education

Bachelor’s Degree or equivalent

Tools

Microsoft Office

Job description

Tennessee Oncology is a community-based cancer care network founded in Nashville, focusing on access to high-quality care and research. This Clinical Trial Specialist I role supports the research team to ensure rigorous adherence to GCP/ICH guidelines while mentoring by more senior staff.

The position involves managing day-to-day trial activities, coordinating with cross-functional teams, and maintaining essential trial documentation to support compliant and efficient studies.