Clinical Research Nurse

Rovia Clinical Research; Anniston (AL); On-site; USD 65,000 - 90,000; Full time

Job summary

Rovia Clinical Research is seeking a Clinical Research Nurse to coordinate ophthalmology trials in compliance with study protocols, ICH/GCP guidelines, and sponsor requirements. This role collaborates with site teams to support startup, enrollment, data integrity, and overall study success.

The candidate must hold RN or LPN licensure and have strong medical terminology knowledge and clinical procedure experience. Experience with EDC/CTMS is a plus, and confidentiality is essential.

Qualifications

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

Responsibilities

• Coordinate and conduct ophthalmology clinical trial visits per protocol.
• Perform clinical tasks such as vitals, EKGs, specimen collection and phlebotomy.
• Obtain informed consent and document it properly.

Skills

Medical terminology

ICH/GCP knowledge

Organizational skills

Interpersonal communication

Multitasking

Microsoft Office

Independence

Patient confidentiality

Education

High school diploma

RN or LPN licensure

Research experience preferred

Tools

EDC

CTMS

Job description

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.
• Resolves data queries and ensures data integrity.
• 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.

Work Schedule: Monday-Thursday 8:00AM-5:00PM, Friday 8:00AM-1:00PM, optional weekends/overnights