Clinical Research Coordinator: Patient-Focused Trials

Rovia; Lake City (FL); On-site; USD 52,000 - 68,000; Full time

Job summary

Rovia Clinical Research in Lake City, FL is seeking a Clinical Research Coordinator to manage and execute trials in accordance with ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

You will coordinate patient visits, collect vitals and samples, ensure informed consent, monitor subject safety, and maintain proper documentation and product accountability, contributing

Qualifications

• High school diploma required.
• 2+ years of clinical research experience.
• Experience with patient-facing activities (phlebotomy, vital signs, EKGs) or ophthalmology tasks preferred.

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, ensuring 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 skills

Multitasking

MS Office

EDC

CTMS

Independent work

Confidentiality

Education

High school diploma

Bachelor's degree

Tools

EDC

CTMS

Job description

Rovia Clinical Research in Lake City, FL is seeking a Clinical Research Coordinator to manage and execute trials in accordance with ICH/GCP guidelines, sponsor requirements, and Rovia SOPs. This role partners closely with site teams to support study startup, enrollment, data quality, and overall study success.

You will coordinate patient visits, collect vitals and samples, ensure informed consent, monitor subject safety, and maintain proper documentation and product accountability, contributing