Clinical Research Coordinator

Universal Axon Clinical Research, LLC; Anniston (AL); Presencial; USD 42 000 - 64 000; Tempo integral

Resumo da oferta

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

Responsibilities include coordinating visits, performing clinical tasks, ensuring proper consent, monitoring safety, and maintaining accurate documentation. A strong focus on patient experience and regulatory compliance is essential.

Qualificações

• Must have a high school diploma.
• Current MA certification or nursing licensure (LPN, RN) preferred.
• Strong knowledge of medical terminology and clinical procedures.
• Familiarity with ICH/GCP and regulatory requirements.

Responsabilidades

• Coordinates patient visits per study protocols.
• Performs vital signs, EKGs, specimen collection and processing as applicable.
• Ensures informed consent is properly obtained and documented.
• Educates and guides participants through the study to ensure a positive experience.
• Monitors subject safety and reports adverse events as appropriate.
• Maintains source documentation and EDC data entry.
• 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.

Conhecimentos

Medical terminology

ICH/GCP knowledge

Organizational skills

Interpersonal communication

Multitasking

Collaboration

Patient confidentiality

Formação académica

High School Diploma

MA certification

Nursing licensure (LPN, RN)

Ferramentas

Microsoft Office

EDC

CTMS

Descrição da oferta de emprego

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.
• Current MA certification or nursing licensure (LPN, RN) preferred.