Rovia Clinical Research

Multispecialty clinical trial site network

Clinical Research Coordinator

Clinical Research OperationsConfirmed live in the last 24 hours

Full-timeJacksonville, FL, USANo salary listed

About the Job

Requirements

Strong knowledge of medical terminology and clinical procedures.
Understanding of International Council for Harmonisation Good Clinical Practice (ICH/GCP) and regulatory requirements.
Strong 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, electronic data capture (EDC), and clinical trial management system (CTMS) applications.
Ability to work both independently and collaboratively.
High level of professionalism and commitment to patient confidentiality.
High school diploma required.
2+ years of clinical research experience.

Responsibilities

Conduct and coordinate patient visits in accordance with study protocols.
Perform clinical tasks such as vital signs, electrocardiograms (EKGs), specimen collection and processing, and phlebotomy as applicable.
Ensure informed consent is properly obtained and documented.
Educate and guide participants through the study, ensuring a positive patient experience.
Monitor subject safety, report adverse events, and escalate concerns as appropriate.
Complete timely and accurate source documentation and electronic data capture (EDC) data entry.
Resolve data queries and ensure data integrity.
Maintain investigational product accountability and proper storage and handling.
Prepare for and support monitoring visits, audits, and inspections.
Collaborate with site staff and investigators to ensure protocol adherence and efficient visit flow.
Perform other duties as assigned.
Be flexible to work at any of Rovia's Jacksonville clinical research sites.

Desired Qualifications

Bachelor’s degree in a related field.

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 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, bachelor’s degree in related field preferred.
2+ years of clinical research experience.

This position requires flexibility to be based at any of Rovia's Jacksonville clinical research sites.

About the Company

Rovia Clinical Research

Multispecialty clinical trial site network

Rovia Clinical Research runs a network of multi-specialty clinical research sites across the United States to conduct clinical trials for drugs, devices, and diagnostics. It uses a hybrid site model that combines fully-owned, stand-alone centers with embedded specialists in independent medical practices to provide on-site trial support. This setup covers study start-up, patient enrollment, data collection and analysis, logistics, training, and business development, helping sponsors run trials more efficiently. Rovia differentiates itself through its scale, diverse patient access, and integrated services that reduce the burden on investigators, accelerated site activation, and a growing investigator network backed by acquisitions and private equity. The company’s goal is to deliver predictable, high-quality trial execution across multiple therapeutic areas by expanding its network and capabilities, serving major pharmaceutical and biotech clients with timely, well-run studies.

Company size: 51-200
Company stage: Not listed
Total funding: Not listed
Headquarters: Jacksonville, FL
Founded: 2007

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