Clinical research scientist vs research project coordinator

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

Clinical research scientist example responsibilities.

• Supervise and manage planning, implementation, conduct and reporting of assign early phase international clinical studies in oncology.
• Facilitate IRB approval, when require.
• Compile and submit reports to U.S. FDA.
• Provide draft responses to FDA questions to senior management.
• Resolve IRB issues and implement IRB mandate changes in the protocol with amendments.
• Recruit investigators perform pre-study visits, negotiate budgets, initiate and monitor studies and verify data for accuracy and completeness.
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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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