Clinical research scientist vs clinical coordinator

Differences between clinical research scientist and clinical 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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Clinical coordinator example responsibilities.

• Manage chronic illnesses such as hypertension, coronary disease and diabetes.
• Create and manage case report forms and transmit data through EDC to sponsor.
• Manage patient telemetries systems to include EKG's, vitals, INR management and sleep monitoring systems.
• Manage the CRA team and serve as main point of contact for study logistics and relate questions including subject eligibility questions.
• Manage common side effects of chemotherapy and experimental therapies.
• Manage the clinical reimbursement coordinators traveling schedule to ensure that facilities have adequate MDS coverage.
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