Clinical Research Coord RN - ORMC - Research
Listed on 2026-07-14
-
Nursing
RN Nurse, Clinical Research Nurse
Company Description
Orlando Health is a not-for-profit healthcare organization serving communities across the southeastern United States. With $7.6 billion in assets under management, the system supports a broad range of advanced clinical services and specialty care. Headquartered in Orlando, Florida, Orlando Health has a history of more than 100 years of providing compassionate, high-quality care. Team members benefit from working in a stable, mission-driven organization that emphasizes patient safety, collaboration, and professional growth.
The system’s long-standing presence in the region offers opportunities for career development within a large, integrated health network.
The Clinical Research Coordinator RN at Orlando Health Orlando Regional Medical Center (ORMC) is a full-time, on-site role based in Orlando, FL. This position coordinates and manages clinical research studies, including patient screening, enrollment, informed consent, and follow-up according to study protocols and regulatory requirements. The role involves collaborating with physicians, nurses, and other research staff to ensure accurate documentation, timely data collection, and adherence to ethical and compliance standards.
The coordinator supports patient education related to study procedures, monitors for adverse events, and communicates with sponsors, regulatory bodies, and institutional review boards. Daily responsibilities also include maintaining study records, preparing reports, and contributing to quality improvement and best practices in clinical research.
- Strong clinical foundation with skills in Nursing and Medicine applicable to patient care within a research environment.
- Competence in Oncology Nursing for roles involving cancer-related clinical trials and patient management.
- Demonstrated ability in Research, including study coordination, data collection, and regulatory compliance.
- Experience working with clinical Protocols, ensuring accurate implementation and documentation of study procedures.
- Active Registered Nurse (RN) license in the state of Florida (or eligibility to obtain), with BSN preferred.
- Prior experience in clinical research, clinical trials, or an academic medical setting is highly beneficial.
- Knowledge of Good Clinical Practice (GCP), FDA regulations, and IRB processes.
- Excellent communication, organizational, and critical‑thinking skills, with attention to detail and patient safety.
- Ability to work collaboratively with multidisciplinary teams and manage multiple studies or tasks simultaneously.
(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).