Clinical research coordinator
Clinical research coordinator
A 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, such as hospitals, universities, and laboratories.
Etymology
The term "Clinical research coordinator" is derived from the English language. "Clinical" (from the Greek word "klinike") refers to the observation and treatment of actual patients, "research" (from the Old French "recercher") means to investigate thoroughly, and "coordinator" (from the Latin "co-" and "ordinare") refers to a person who organizes and harmonizes actions or efforts.
Roles and Responsibilities
The primary responsibility of a Clinical research coordinator is to manage and oversee clinical trials. They work closely with principal investigators to ensure that all aspects of the trials comply with the protocols established by the sponsoring organization, such as pharmaceutical or biotechnology companies, and regulatory authorities. Their duties include participant recruitment, informed consent process, data collection and management, adverse event reporting, and ensuring the overall integrity of data.
Related Terms
- Clinical Trial: A type of research that studies new tests and treatments and evaluates their effects on human health outcomes.
- Principal Investigator: The person who is in charge of a clinical trial or research grant.
- Informed Consent: A process in which a healthcare provider educates a patient about the risks, benefits, and alternatives of a given procedure or intervention.
- Adverse Event: An unexpected medical problem that happens during treatment with a drug or other therapy.
- Data Management: The process of collecting, storing, and using data securely, efficiently, and cost-effectively.
See Also
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