Clinical Research Coordinator organizes research information for clinical projects. Selects and observes subjects and assists with data analysis and reporting. Being a Clinical Research Coordinator oversees experiment scheduling and collection of data. Requires a high school diploma or equivalent. Additionally, Clinical Research Coordinator typically reports to a supervisor or manager. The Clinical Research Coordinator works under moderate supervision. Gaining or has attained full proficiency in a specific area of discipline. To be a Clinical Research Coordinator typically requires 1-3 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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