Job Description
Company Description
Research Institute of Orlando (RIO), LLC specializes in FDA-regulated clinical research trials. We focus on Neurology and Healthy patient trials from around the world. Our mission is to facilitate the development of regulated medications through the participation of our patients. Our dedication drives us to deliver top-notch clinical research and innovation. Role Description
This is a full-time on-site role for a Clinical Research Coordinator, located in Orlando, FL. The Clinical Research Coordinator will be responsible for the day-to-day management of clinical trials, including obtaining informed consent, ensuring protocol adherence, coordinating patient visits, and maintaining accurate study records. The role involves close interaction with patients and research staff, overseeing the execution of clinical research protocols, and ensuring compliance with regulatory requirements.
Qualifications
- Informed Consent and Protocol management skills
- Experience in Clinical Research and Clinical Trials
- Strong understanding of research methodologies and compliance regulations
- Excellent communication and organizational skills
- Ability to work independently and as part of a team
- Prior experience in a clinical research setting is beneficial
- Bachelor's degree in a related field (e.g., Life Sciences, Medicine, Nursing) is preferred
Job Tags
Full time,