Clinical research administrator vs research project coordinator

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

Clinical research administrator example responsibilities.

• Manage regional academic and community base oncology practices as the primary contact for all communications and support.
• Ensure effective data management and the following of good clinical practice (GCP) guidelines.
• Initiate the development of standard operating procedures for regulatory compliance monitoring and auditing of regulatory and IRB documentation.
• Assist with reports and documents to FDA.
• Train new site personnel on specific clinical trial procedures and appropriate FDA regulations.
• Develop and implement program for continual review and quality assessment of regulatory and IRB documentation.
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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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