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 managing and executing 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. • Experience with patient-facing activities (phlebotomy, vital signs, EKGs, etc.) or ophthalmology tasks (OCT imaging, measuring IOP, etc.) strongly preferred.