Onsite Clinical Research Coordinator - Oncology Trials

Florida Clinical Trials Group; Plantation (FL); Vor Ort; USD 32.000 - 45.000; Vollzeit

Zusammenfassung

Florida Clinical Trials Group is seeking a Clinical Research Coordinator for a full-time, on-site role in Plantation and Tamarac, FL. You will coordinate patient recruitment, schedule visits, obtain informed consent, and maintain trial documentation while supporting investigators in procedures.

The role emphasizes data collection/entry, source verification, regulatory file upkeep, and sponsor/CRO communication, with a focus on GCP compliance and patient safety.

Qualifikationen

• Accountable and responsible for assigned studies, patients, deadlines and follow-up.
• Proactive and anticipates what needs to happen next rather than waiting for reminders.
• Reliable with important tasks, communications, documentation and follow-ups.
• Organized to manage multiple patients, protocols, vendors, deadlines, and priorities.
• Communicative, escalates concerns early and keeps the team informed.
• Adaptable to a growing organization where priorities evolve.
• Committed to contributing, learning and improving processes together.

Aufgaben

• Coordinate day-to-day clinical trial activities including patient recruitment, visit scheduling and documentation.
• Obtain and document informed consent and ensure adherence to study protocols.
• Support investigators in clinical procedures and conduct.
• Perform data collection/entry, source document verification and regulatory file maintenance.
• Communicate with sponsors and CROs and monitor participant safety.
• Report adverse events and ensure compliance with GCP and applicable regulations.

Kenntnisse

Accountable

Proactive

Solution-oriented

Reliable

Organized

Communicative

Adaptable

Committed

Jobbeschreibung

Florida Clinical Trials Group is seeking a Clinical Research Coordinator for a full-time, on-site role in Plantation and Tamarac, FL. You will coordinate patient recruitment, schedule visits, obtain informed consent, and maintain trial documentation while supporting investigators in procedures.

The role emphasizes data collection/entry, source verification, regulatory file upkeep, and sponsor/CRO communication, with a focus on GCP compliance and patient safety.