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IMARC Blog

Compliance In Focus

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Posted by John Lehmann on Wed, Mar 04, 2015

How to Improve Individual Site Compliance

Topics: Site Compliance, Training, Investigator, Study Team, IMARC Research

Posted by John Lehmann on Wed, Mar 04, 2015

How to Improve Individual Site Compliance

In order to run a well-controlled compliant study at the site level, one must ensure that the study team has been trained, and is knowledgeable on the rules and regulations. Although it is the Investigator who is responsible for the conduct of the study, there is a larger team at work to complete all the required activities. The research coordinator carries out many of the day-to-day activities and touches nearly every study milestone.

Topics: Research Coordinator, Site Compliance, Investigator, IMARC Research

Posted by Jacqui Lingler on Wed, Mar 04, 2015

How to Improve Individual Site Compliance

Topics: Research Coordinator, Site Compliance, Training, IMARC Research

Posted by Brandy Smith on Wed, Mar 04, 2015

How to Improve Individual Site Compliance

In order to run a well-controlled compliant study at the site level, one must ensure that the study team has been trained, and is knowledgeable on the rules and regulations. Although it is the Investigator who is responsible for the conduct of the study, there is a larger team at work to complete all the required activities. The research coordinator carries out many of the day-to-day activities and touches nearly every study milestone.

Topics: Site Compliance, Whitepaper, Improve Site Compliance, IMARC Research

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Clinical Research Training Requirements
Featured Resource

clinical research Training requirements

This whitepaper examines the similarities and differences between various US and international regulations and place them within the context of any number of roles found within the realm of clinical research.