Clinical Informatics Coordinator is responsible for the creation, implementation, and analysis of data and information systems required for patient care initiatives. Works with healthcare providers to identify useful clinical data and establish methods of collecting and storing it. Being a Clinical Informatics Coordinator performs analyses to create insights and identify patterns and areas for improvement. Communicates with providers and management to learn the organization's processes and priorities, and to provide takeaways in the most accessible and convenient way possible. Additionally, Clinical Informatics Coordinator typically requires a bachelor's degree. Typically reports to a manager or head of a unit/department. The Clinical Informatics Coordinator work is generally independent and collaborative in nature. Contributes to moderately complex aspects of a project. To be a Clinical Informatics Coordinator typically requires 4-7 years of related experience. (Copyright 2024 Salary.com)
Job Summary:
The Research Coordinator manages protocols to ensure the safety of patients, quality of clinical trial data and compliance with facility, system and Federal Research regulations through oversight of Institutional Review Board (IRB) paperwork, maintenance of all related regulatory document submissions and communication/coordination of study activities with the Primary Investigator and any Sub-Investigators of clinical studies.
Job Requirements:
Bachelor’s degree required. Health-related field preferred.
Research and Data Management experience required.
Certification in clinical research (SoCRA, ACRP) preferred.
Working knowledge of Microsoft Office Suite (Outlook, Word, Excel, PowerPoint, and Access) and a wide variety of software applications.
Proficiency in the review and abstraction of clinical patient information from a medical record.
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