Clinical Research Nurse

Rovia Clinical Research

Anniston (AL)

On-site

USD 60,000 - 80,000

Full time

6 days ago
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Job summary

Rovia Clinical Research in Anniston, Alabama, is seeking a Clinical Research Nurse to coordinate ophthalmology trials in accordance with ICH/GCP guidelines and sponsor requirements.

This role partners with site teams to support trial startup, enrollment, data quality, and overall study success, performing patient visits, vital signs, phlebotomy, and accurate data entry while maintaining compliance and patient confidentiality.

Qualifications

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

Responsibilities

  • Coordinate ophthalmology clinical visits per study protocol.
  • Perform clinical tasks: vitals, ECGs, specimen collection and processing, phlebotomy as applicable.
  • Ensure informed consent is obtained and documented.
  • Educate and guide participants to ensure positive patient experience.
  • Monitor subject safety and report adverse events.
  • Complete source documentation and EDC data entry.
  • Maintain investigational product accountability and storage.
  • Prepare for monitoring visits, audits and inspections.
  • Collaborate with site staff to ensure protocol adherence and efficient visit flow.
  • Perform other duties as assigned.

Skills

RN/LPN licensure
Ophthalmology knowledge
Clinical data entry
Regulatory knowledge
Organizational skills
Interpersonal skills
Microsoft Office/EDC/CTMS
Independent & collaborative
Patient confidentiality

Education

RN or LPN licensure
High school diploma
Research experience preferred

Job description

Clinical Research Nurse

Rovia Clinical Research Anniston, Alabama, United States

About this position

About Us

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.
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