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This recorded, self-paced course provides 24/7 access to practical, hands-on training for those interested in gaining knowledge about monitoring in the oncology therapeutic area. As demand for CRAs in the oncology arena continues to grow, this course offers practical, hands-on training covering oncology-specific logistical, clinical and ethical considerations. The application of clinical monitoring skills is reinforced through core content, exercises, case studies, and practice based activities. The course also includes an application-based post-course exam, and once successfully completed, a certificate is provided.
Course Learning Objectives- Manage challenges associated with oncology trials
- Describe common characteristics of the Institutional Review Board (IRB) review and communications in oncology trials
- Examine approaches for decision-making at sites for dosing toxicities and dose modification
- Apply standardized grading criteria to adverse events in oncology studies
- Establish strategies for source documentation and monitoring visits
Key Features Include: - Application-based exercises and examples
- Focus on practical application of principles and job functions
- Knowledge checks, assessments and post-course exam
- Includes a Barnett certificate of training
- Applicable for global clinical research professionals