Clinical research monitor vs research project coordinator

Differences between clinical research monitor and research project coordinator duties and responsibilities

Clinical research monitor example responsibilities.

• Manage a consultant to review scientific support and create dossiers on each product that make health claims in the EU.
• Maintain CTMS project tracking system of subject and site information and essential documents.
• Collect and review all initial regulatory documents from site for submission to IRB and sponsor.
• Coordinate and conduct the training of site personnel on protocols, CRF review and conduct source document verification.
• Resolve CRF discrepancies and/or clarifications via site visit, telephone, email or fax as deemed appropriate for the study.
• Prepare high quality site documents and collect country-specific information for IRB processes.
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Research project coordinator example responsibilities.

• Manage study documentation throughout study life cycle including IRB annual renewals, modifications, patient study charts and regulatory binder.
• Recommend administrative revisions to IRB submit studies including inform consent documents.
• Demonstrate small molecule are protective against DNA damage in mouse model of melanoma.
• Conduct analysis using SPSS which result in developing a new software for students to selecting college.
• Conduct primary research through interviews with Boston area travelers and analyze raw data into reports via SPSS.
• Maintain FDA correspondence and government documentation.
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