Clinical Research Coordinator

Rovia Clinical Research; Jacksonville (FL); Sur place; USD 52 000 - 72 000; Plein temps

Résumé du poste

Rovia Clinical Research is seeking a Clinical Research Coordinator to manage ophthalmology trials in accordance with ICH/GCP guidelines. You will work with site teams to support startup, enrollment, data quality, and overall study success.

Responsibilities include coordinating patient visits, performing clinical tasks, ensuring informed consent, and maintaining source documentation. The role requires strong organization, communication, and a patient-focused approach at our Jacksonville sites.

Qualifications

• Minimum 2 years of clinical research experience.
• Bachelor’s degree in a related field preferred.
• Strong knowledge of ICH/GCP and regulatory requirements.
• Excellent organizational and patient-facing communication skills.

Responsabilités

• Coordinate patient visits per study protocol.
• Perform vital signs, EKGs, sample collection and processing as applicable.
• Ensure informed consent is properly obtained and documented.
• Educate participants and ensure a positive patient experience.
• Monitor subject safety and report adverse events.
• Maintain source documentation and EDC data entry.
• Support monitoring visits, audits, and inspections.
• Collaborate with site staff to ensure protocol adherence.

Connaissances

Medical terminology

ICH/GCP knowledge

Organizational skills

Interpersonal skills

Multitasking

MS Office

EDC proficiency

CTMS experience

Independent & collaborative

Patient confidentiality

Formation

High school diploma

Bachelor's degree preferred

Outils

EDC

CTMS

MS Office

Description du poste

At Rovia Clinical Research, we’re on a mission to bring innovative treatments to patients, improving the health and lives of our local patient communities. We believe in building a workplace where people feel supported, valued, and excited to grow their careers. Whether you’re just starting out or looking for a new path, you’ll be part of a team that truly works together and makes an impact. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability.

Position Summary:

The Clinical Research Coordinator is responsible for coordinating and executing ophthalmology clinical trials in accordance with study protocols, 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.

Key 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/Abilities:

• Strong knowledge of medical terminology and clinical procedures.
• Understanding of ICH/GCP and regulatory requirements.
• Excellent organizational skills and attention to detail.
• Strong interpersonal and patient-facing communication skills.
• Ability to multitask and manage competing priorities in a fast-paced environment.
• Proficiency in Microsoft Office, EDC, and CTMS applications.
• Ability to work both independently and collaboratively.
• High level of professionalism and commitment to patient confidentiality.

Education/Experience:

• High school diploma required, bachelor’s degree in related field preferred.
• 2+ years of clinical research experience.

This position requires flexibility to be based at any of Rovia's Jacksonville clinical research sites.