Clinical Research Coordinator

Florida Clinical Trials Group; Miami, Fort Lauderdale (FL, FL); On-site; USD 39,000 - 50,000; Full time

Job summary

Florida Clinical Trials Group is seeking a Clinical Research Coordinator who is ready to contribute to a growing oncology research organization. The role requires understanding the core responsibilities of clinical trial coordination and a proactive, accountable approach.

We value someone who is reliable, organized, communicative and adaptable as our studies evolve. Previous oncology experience is strongly preferred and will help you hit the ground running, assist investigators, manage

Qualifications

• Understanding of core responsibilities of clinical trial coordination.
• Ability to manage patient flow, deadlines, and follow-up.
• Strong communication with investigators and study team.

Responsibilities

• Coordinate clinical trial activities across assigned studies.
• Support patient enrollment and follow-up procedures.
• Maintain study documents, deadlines and study team communications.

Skills

Accountable

Proactive

Solution-oriented

Reliable

Organized

Communicative

Adaptable

Committed

Job description

Florida Clinical Trials Group is seeking aClinical Research Coordinatorwho is ready to contribute to a growing oncology research organization.

Anyone applying for a CRC position should already understand the core responsibilities of clinical trial coordination. What matters most to us ishow you approach those responsibilities.

We are looking for someone who is:

• Accountable:Takes responsibility for assigned studies, patients, deadlines, and follow-up.
• Proactive:Anticipates what needs to happen next rather than waiting to be reminded.
• Solution-oriented:Identifies problems early and, whenever possible, proposes a path forward.
• Reliable:Important tasks, communications, documentation, and follow-ups do not get forgotten.
• Organized:Can manage multiple patients, protocols, vendors, deadlines, and competing priorities.
• Communicative:Escalates concerns early and keeps investigators and the study team informed.
• Adaptable:Comfortable working in a growing organization where priorities may evolve quickly.
• Committed:Looking for a position where they can contribute, learn, improve processes, and grow with the organization.

Previousoncology clinical research experience is strongly preferred, and experience with complex interventional or early-phase studies is particularly valuable.

At Florida Clinical Trials Group, we want team members whohelp build a stronger clinical research operation.

Compensation: Starting at $28/hour, based on relevant experience.