On-Demand 30-Hour Monitoring Oncology Clinical Trials Program - $1995.00

Too Busy To Attend A Course?
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.

• 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

• 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