Clinical Research Coordinator
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Job Description
Florida Clinical Trials Group is seeking a Clinical Research Coordinator who 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 is how 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.
Previous oncology 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 who help build a stronger clinical research operation.
Compensation: Starting at $28/hour, based on relevant experience.