Clinical Trial Coordinator: Patient Care & Data Quality

Rovia Clinical Research; Lake City (FL); On-site; USD 48,000 - 60,000; Full time

Job summary

Rovia Clinical Research in Lake City, Florida, is seeking a Clinical Research Coordinator to manage patient visits, perform essential clinical tasks, and ensure informed consent is properly obtained.

The role supports study startup, enrollment, data quality, and overall trial success while adhering to ICH/GCP guidelines and sponsor SOPs. A strong clinical background and patient-facing skills are essential for success.

Qualifications

• 2+ years of clinical research experience.
• Strong knowledge of medical terminology and clinical procedures.
• Understanding of ICH/GCP and regulatory requirements.
• Excellent organizational and patient-facing communication skills.

Responsibilities

• Conducts and coordinates patient visits in accordance with study protocols.
• Performs clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable.
• Ensures informed consent is properly obtained and documented.
• Educates and guides participants through the study for a positive patient experience.
• Monitors subject safety, reports adverse events, and escalates concerns as appropriate.
• Completes timely and accurate source documentation and EDC data entry.
• Maintains investigational product accountability and proper storage and handling.
• Prepares for and supports monitoring visits, audits, and inspections.
• Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
• Perform other duties as assigned.

Skills

Medical terminology

ICH/GCP

Organizational skills

Interpersonal communication

Multitasking

MS Office

EDC

CTMS

Independent work

Confidentiality

Education

High school diploma

Bachelor's degree preferred

Tools

Microsoft Office

EDC

CTMS

Job description

Rovia Clinical Research in Lake City, Florida, is seeking a Clinical Research Coordinator to manage patient visits, perform essential clinical tasks, and ensure informed consent is properly obtained.

The role supports study startup, enrollment, data quality, and overall trial success while adhering to ICH/GCP guidelines and sponsor SOPs. A strong clinical background and patient-facing skills are essential for success.