Clinical Research Coordinator 1

Clinical Research Coordinator 1 Rovia Clinical Research, Canton, Georgia, United States – Medical About this position 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. Our team is driven by our core values: People First, Humility, Integrity, One Team, and Results Accountability. Position Summary The Clinical Research Coordinator 1 (CRC) is responsible for coordinating 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 Conduct patient visits in accordance with study protocols. Perform clinical tasks such as vital signs, 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 escalates concerns as appropriate. Complete timely and accurate source documentation and 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. 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 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. At least 1 year of clinical research experience. Experience with patient‑facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred. The pay range for this role is: 50,000 - 55,000 USD per year (Canton) #J-18808-Ljbffr