Clinical Research Coordinator
Clinical Research Coordinator
The Clinical Research Coordinator (pronounced klin-i-kal ri-surch ko-or-di-nay-tor) is a healthcare professional who plays an integral role in medical research settings. They are primarily responsible for organizing, managing, and ensuring the integrity of clinical trials.
Etymology
The term "Clinical Research Coordinator" is derived from the English language. "Clinical" refers to the observation and treatment of actual patients rather than theoretical or laboratory studies. "Research" is the systematic investigation into and study of materials and sources to establish facts and reach new conclusions. "Coordinator" refers to a person whose job is to organize events or activities and to negotiate with others in order to ensure they work together effectively.
Roles and Responsibilities
A Clinical Research Coordinator is involved in every aspect of clinical trials. They work closely with the principal investigator, assisting in participant recruitment, obtaining informed consent, scheduling and conducting study visits, and maintaining accurate documentation. They also ensure compliance with regulatory standards and ethical guidelines.
Related Terms
Education and Training
Typically, a Clinical Research Coordinator holds a bachelor's degree in a health-related field. They may also have additional certifications or training in clinical research. Many Clinical Research Coordinators are registered nurses or have other medical backgrounds.
See Also
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