Bilingual Clinical Research Coordinator - Patient Trials

Rovia; Miami (FL); On-site; USD 52,000 - 78,000; Full time

Job summary

Rovia Clinical Research seeks a bilingual Clinical Research Coordinator to manage patient visits, collect data, and ensure protocol adherence under ICH/GCP guidelines.

The role requires 2+ years in clinical research, ability to coordinate with site teams, and proficiency in Microsoft Office, EDC, and CTMS. Fluency in English and Spanish is essential for patient interactions and regulatory communications.

Qualifications

• High school diploma required; bachelor’s degree preferred.
• 2+ years of clinical research experience.
• Experience with patient-facing activities preferred.

Responsibilities

• Coordinate patient visits per study protocol.
• Perform vital signs, EKGs, specimen collection as applicable.
• Ensure informed consent is documented.
• Support monitoring visits, audits, and inspections.
• Maintain source documentation and data entry.

Skills

Clinical Procedures

ICH/GCP

Data Entry

Multitasking

Regulatory Knowledge

Bilingual EN/ES

Education

Bachelor’s degree preferred

High school diploma required

Tools

Microsoft Office

EDC

CTMS

Job description

Rovia Clinical Research seeks a bilingual Clinical Research Coordinator to manage patient visits, collect data, and ensure protocol adherence under ICH/GCP guidelines.

The role requires 2+ years in clinical research, ability to coordinate with site teams, and proficiency in Microsoft Office, EDC, and CTMS. Fluency in English and Spanish is essential for patient interactions and regulatory communications.