Senior Clinical Research Associate
About this role
Senior Clinical Research Associate
What you will do
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Responsible for site qualification, initiation, interim monitoring, site management, and study close-out visits.
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Provide mentoring and guidance to less experienced CRAs and site staff when needed.
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Document site visit findings via written reports.
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Assess, monitor, and train study site staff on protocol adherence as required.
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Review study subject safety information and informed consent.
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Conduct source document verification for compliance, patient safety, and veracity of data.
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Review CRFs using paper or electronic data capture systems and assist sites with data query resolution.
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Provide applicable updates for site related documentation for filing in the Trial Master File (TMF).
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Ensure site compliance with IP receipt, accountability and return or destruction.
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