Clinical Research Coordinator I – On-site (Florida)

American Oncology Network; Naples (FL); On-site; USD 25,000 - 39,000; Full time

Job summary

The American Oncology Network is seeking a Clinical Research Coordinator I (non-RN) to oversee the execution and ongoing management of multiple clinical trials in a fast-paced, multi-site environment. You will coordinate patient care on protocols, ensure regulatory compliance, and support data integrity while working under physician supervision.

Key duties include protocol feasibility, patient screening, adverse event reporting, and collaboration with the sponsor, IRB, and study team.

Qualifications

• High school education required; some college preferred.
• Prior research or related medical science experience.
• Proficiency in MS Office; EMR/EDC/CTMS experience encouraged.
• Strong communication and ability to work remotely as required.

Responsibilities

• Coordinate care for patients on clinical research protocols per GCP/ICH guidelines.
• Identify inclusion/exclusion criteria and conduct prescreening and screening tasks.
• Review diagnostic tests and informed consent documentation.
• Document adverse events and report to sponsor/IRB as needed.
• Maintain regulatory compliance and data integrity across studies.
• Assist with budgeting, contracts, and study-related financial practices.

Skills

Analytical thinking

Interpersonal skills

Communication

Customer service

Self-management

Education

High school diploma

Some college

Tools

MS Office

EMR

EDC

CTMS

Job description

The American Oncology Network is seeking a Clinical Research Coordinator I (non-RN) to oversee the execution and ongoing management of multiple clinical trials in a fast-paced, multi-site environment. You will coordinate patient care on protocols, ensure regulatory compliance, and support data integrity while working under physician supervision.

Key duties include protocol feasibility, patient screening, adverse event reporting, and collaboration with the sponsor, IRB, and study team.