Clinical Research Coordinator

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

Job summary

Rovia Clinical Research in Anniston, AL is seeking a Clinical Research Coordinator to coordinate ophthalmology trials in line with study protocols and regulatory standards. You will work with site teams to support startup, enrollment, data quality, and overall study success.

The role requires knowledge of medical terminology, ICH/GCP, and strong organizational and patient-facing communication skills. High school diploma is required; MA/nursing licensure is preferred.

Qualifications

• High school diploma required.
• MA certification or nursing licensure (LPN, RN) preferred.

Responsibilities

• Coordinates patient visits according to study protocols.
• Performs clinical tasks such as vital signs, EKGs, specimen collection & processing.
• Ensures informed consent is properly obtained and documented.
• Educates and guides participants through the study for a positive experience.
• Monitors subject safety and reports adverse events as needed.
• Completes source documentation and EDC data entry accurately.
• Resolves data queries and ensures data integrity.

Skills

Medical terminology

ICH/GCP

Organization

Interpersonal communication

Multitasking

Microsoft Office

EDC

CTMS

Independent & collaborative

Confidentiality

Education

High school diploma

MA certification or nursing licensure (LPN/RN) preferred

Tools

Microsoft Office

EDC

CTMS

Job description

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

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

Work Schedule:

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