Employment Agreement between Clinical Trial Firm and Clinical Research Coordinator. The Clinical Research Coordinator (CRC) is a specialized research professional working with and under the direction of the clinical Principal Investigator (PI). While the Principal Investigator is primarily responsible for the overall design, conduct, and management of the clinical trial, the CRC supports, facilitates and coordinates the daily clinical trial activities and plays a critical role in the conduct of the study. By performing these duties, the CRC works with the PI, department, sponsor, and institution to support and provide guidance on the administration of the compliance, financial, personnel and other related aspects of the clinical study.
Employment Agreement - Clinical Research Coordinator and Clinical Trial Firm
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How to fill out Employment Agreement - Clinical Research Coordinator And Clinical Trial Firm?
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FAQ
The average salary for a clinical research coordinator in the United States is around $112,044 per year.
Clinical coordinators in the United States make an average salary of $53,021 per year or $25.49 per hour. People on the lower end of that spectrum, the bottom 10% to be exact, make roughly $37,000 a year, while the top 10% makes $75,000. As most things go, location can be critical.
Did you know that the average clinical trial coordinator makes $50,117 per year? That's valued at $24.09 per hour! The range surrounding that average can vary between $35,000 and $70,000, meaning clinical trial coordinators have the opportunity to earn more once they move past entry-level roles.
The Clinical research associate or CRA will review and verify all the materials on the day of closure of the clinical trial. The clinical research coordinator helps archive all the documents at the site when the verification by CRA is complete.
Clinical Research Coordinators work under Clinical Research Managers and are tasked with administering clinical trials. Their primary responsibilities include managing clinical trials and collecting data, informing participants about study objectives, and administering questionnaires.
A great CRC possesses excellent verbal and written communication skills. Ensure Participant Understanding: When communicating with participants, the CRC should be able to explain a complex research protocol at the patient's level of understanding.
Research coordinators ensure study subjects meet the criteria set forth by the organization they work for. They also address any concerns or problems the subjects might have prior to and during the study.
Clinical research coordinators carefully organize clinical studies to produce the most accurate results possible. They maintain critical, legal records of what goes on during studies, including case reports and drug dispensation records. Their data is essential in determining the success or failure of a therapy.