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.

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
 

30 hr Oncology