Clinical Research Coordinator

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
• Results Accountability

Position Summary

The Clinical Research Coordinator (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 and coordinate 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 escalate 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 both independently and collaboratively.
• High level of professionalism and commitment to patient confidentiality.

Education/Experience

• High school diploma required; bachelor’s degree in a related field preferred.
• At least 1 year of clinical research experience.
• Experience with patient‑facing activities (phlebotomy, vital signs, EKGs, etc.) strongly preferred.