Clinical Research Coordinator – 24/7 Acute Care Trials

Virginia Commonwealth University; Virginia (MN); Vor Ort; USD 55.000 - 69.000; Vollzeit

Benefits dieser Stelle

Health benefits

Tuition benefits

Retirement plan

Paid leave

Zusammenfassung

Virginia Commonwealth University in Virginia is seeking a Clinical Research Coordinator to support cross-departmental trials within the School of Medicine's Neurosurgery section. The role focuses on enrollment, data management, and regulatory duties, with a rotating schedule including nights, weekends, and holidays.

The position emphasizes coordination of clinical trials across departments, adherence to GCP/IRB requirements, and collaboration with senior staff to ensure compliant study conduct

Qualifikationen

• Bachelor's Degree or equivalent related experience.
• Ability to prioritize work requirements and multi-task in fast-paced environment.
• Excellent organization and communication skills.
• Experience in clinical research preferred.
• Multilingual skills preferred.

Aufgaben

• Assist in subject recruitment: pre-screening and screening.
• Enrollment of eligible study participants.
• Conduct the informed consent process.
• Monitor patients within VCU Health during participation and follow-up.
• Access data capture/retrieval systems to identify potential study participants.
• Supervise per diem CRCs and assist with scheduling duties.
• Maintenance of study documents according to GCP.
• Support the PI and senior staff in following participants through all study activities.
• Assist with required study close-out activities.

Kenntnisse

Attention to detail

Communication

Organization

Teamwork

Flexibility

Prioritization

Ausbildung

Bachelor's Degree or equivalent

Master's Degree (preferred)

Tools

RedCap

EPIC

OnCore

Microsoft Programs

Jobbeschreibung

Virginia Commonwealth University in Virginia is seeking a Clinical Research Coordinator to support cross-departmental trials within the School of Medicine's Neurosurgery section. The role focuses on enrollment, data management, and regulatory duties, with a rotating schedule including nights, weekends, and holidays.

The position emphasizes coordination of clinical trials across departments, adherence to GCP/IRB requirements, and collaboration with senior staff to ensure compliant study conduct