Clinical Trials Coordinator – Research & Coordination

CAMC Health System; Charleston (WV); Vor Ort; USD 60.000 - 85.000; Vollzeit

Zusammenfassung

CAMC Health System is seeking a Clinical Research Coordinator to manage all aspects of clinical trials, from protocol development to data collection and regulatory compliance. This role interfaces with sponsors, physicians and multiple departments to ensure study success and patient safety.

The successful candidate will support IRB submissions, coordinate visits and procedures, monitor study progress, and help maintain budgets and documentation in a fast-paced, governed environment.

Qualifikationen

• Master's degree or equivalent with relevant clinical research experience.
• CCRP credential is preferred but not required.

Aufgaben

• Coordinate all aspects of clinical research trials as assigned.
• Manage sponsor, physician, department and staff relationships.
• Oversee protocol requirements, data collection, and regulatory documentation.
• Assist with IRB submissions and regulatory processes.
• Ensure compliance with approved protocols and quality standards.
• Maintain study budgets, tracking payments and study progress.

Ausbildung

Master's Degree

CCRP credential

Jobbeschreibung

CAMC Health System is seeking a Clinical Research Coordinator to manage all aspects of clinical trials, from protocol development to data collection and regulatory compliance. This role interfaces with sponsors, physicians and multiple departments to ensure study success and patient safety.

The successful candidate will support IRB submissions, coordinate visits and procedures, monitor study progress, and help maintain budgets and documentation in a fast-paced, governed environment.