Clinical Research Coordinator — Protocols & Data

Florida Onc; Fort Myers (FL); On-site; USD 59,543,000 - 104,623,000; Full time

Job summary

Florida Oncology and Hematology is seeking a Clinical Research Coordinator I (non-RN) to oversee study implementation under PI supervision. The role covers protocol coordination, regulatory adherence, data integrity, and billing compliance across multiple trials in a fast-paced multi-site environment.

Responsibilities include patient screening, informed consent processes, adverse event reporting, and collaboration with research staff. Remote work may be required as needed.

Qualifications

• High school education is required; some college preferred.
• Prior research or related medical science experience.
• Detail oriented with ability to exercise independent judgment.
• Ability to work remotely effectively as required.

Responsibilities

• Coordinate care for patients on clinical research protocols.
• Manage regulatory and data integrity responsibilities.
• Assist with budget/contract elements and billing compliance.
• Prepare documents for monitoring visits.
• Follow GCP and FDA guidelines.

Skills

GCP knowledge

IRB/IEC regulatory compliance

Data entry / EDC systems

MS Office proficiency

Communication skills

Time management

Remote work capability

Education

High school diploma

Some college preferred

Tools

EMR software

EDC systems

CTMS

Job description

Florida Oncology and Hematology is seeking a Clinical Research Coordinator I (non-RN) to oversee study implementation under PI supervision. The role covers protocol coordination, regulatory adherence, data integrity, and billing compliance across multiple trials in a fast-paced multi-site environment.

Responsibilities include patient screening, informed consent processes, adverse event reporting, and collaboration with research staff. Remote work may be required as needed.