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- CCRP® Certified Clinical Research Professional
Curriculum
- 3 Sections
- 18 Lessons
- 40 Hours
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- Domain 1: Research Study Start-Up7
- 1.1Oversee the development and initiation of the research study protocol.
- 1.2Prepare or acquire all necessary study documentation.
- 1.3Secure approvals from relevant stakeholders for the study.
- 1.4Procure study-related materials, equipment, tools, and aids.
- 1.5Identify and select appropriate research study sites.
- 1.6Conduct training sessions for research staff members.
- 1.7Assess and ensure compliance with research protocols and guidelines.
- Domain 2: Research Study Implementation7
- 2.1Carry out the execution of the research study in accordance with the protocol.
- 2.2Ensure adherence to all regulatory and compliance standards.
- 2.3Manage and oversee the use of research study products.
- 2.4Identify, document, and address any anomalies or deviations in the study.
- 2.5Supervise the management of research subjects.
- 2.6Maintain the integrity of the research study through continuous monitoring.
- 2.7Facilitate effective communication with all stakeholders involved in the study.
- Domain 3: Research Study Closure4
- 3.1Conduct the study closeout visit in alignment with study requirements.
- 3.2Perform audits to ensure the research study’s accuracy and compliance.
- 3.3Prepare and submit comprehensive closure reports for the research study.
- 3.4Archive and manage retrieval of all research study records for future reference.
Prepare or acquire all necessary study documentation.
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