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INFORMATION PACKET 2013 ? 2014 For more information, contact Regina Ponder, Exec. J.D., C.C.R.P. Program Director at 602.286.8488 CLINICAL RESEARCH COORDINATOR Certificate of Completion in Clinical
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What is clinical research coordinator?
A clinical research coordinator is a healthcare professional responsible for overseeing and coordinating clinical research studies. They act as a liaison between investigators, sponsors, and participants, ensuring that the study is conducted in compliance with regulations and protocols.
Who is required to file clinical research coordinator?
Clinical research coordinators are not required to file any specific documents. However, they are responsible for collecting and maintaining the necessary documentation and data related to the clinical research study they are coordinating.
How to fill out clinical research coordinator?
Filling out clinical research coordinator forms or documents would depend on the specific requirements of the institution or organization conducting the study. The coordinator must ensure all relevant information regarding the study participants, protocols, and data collection is accurately recorded and organized.
What is the purpose of clinical research coordinator?
The purpose of a clinical research coordinator is to ensure the smooth and efficient conduct of a clinical research study. They are responsible for various tasks such as participant recruitment, consent procedures, data collection, and regulatory compliance.
What information must be reported on clinical research coordinator?
The specific information that must be reported on a clinical research coordinator form or document will depend on the requirements of the study and the organization conducting it. Generally, information such as participant demographics, medical history, study procedures, adverse events, and data collection details may need to be reported.
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