Clinical Research Nurse

Universal Axon Clinical Research, LLC; Anniston (AL); On-site; USD 55,000 - 75,000; Full time

Job summary

Rovia Clinical Research in Anniston, AL is seeking a Clinical Research Nurse to coordinate ophthalmology trials following ICH/GCP and sponsor SOPs. This on-site role partners with site teams to support startup, enrollment, data quality, and overall study success.

You will perform clinical tasks such as vital signs, EKGs, specimen collection and processing, and phlebotomy as applicable. Must hold RN or LPN licensure and a high school diploma; research experience is preferred.

Qualifications

• High school diploma required.
• Current RN or LPN licensure required.
• Research experience preferred.

Responsibilities

• Coordinates patient visits according to study protocols.
• Performs clinical tasks (vital signs, EKGs, specimen collection) as applicable.
• Ensures informed consent is properly obtained and documented.
• Educates and guides participants through the study and ensures a positive patient experience.
• Monitors subject safety, reports adverse events, and escalates concerns as needed.
• Completes source documentation and EDC data entry.
• Maintains investigational product accountability and storage.
• Prepares for and supports monitoring visits, audits, and inspections.
• Collaborates with site staff and investigators to ensure protocol adherence and efficient visit flow.
• Performs other duties as assigned.

Skills

Medical terminology

ICH/GCP

Organizational skills

Interpersonal communication

Multitasking

Microsoft Office

EDC

CTMS

Independence

Teamwork

Education

High school diploma

RN or LPN licensure

Tools

EDC

CTMS

Job description

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 Nurse 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.
• Current LPN or RN licensure required.
• Research experience preferred.