Oncology clinical trials are crucial for the development of new treatments and therapies for cancer. The "Oncology Clinical Trials From Design to Implementation" course offers a comprehensive guide to the various stages involved in conducting clinical trials specifically for oncology. The course begins with an introduction to the significance of oncology clinical trials, providing an overview of historical milestones, ethical considerations, and the regulatory framework in the UK. Students will then learn the intricacies of designing clinical trials, covering various phases, protocol development, patient recruitment, and eligibility criteria.

The course delves into data collection and management, ensuring students understand the tools and methodologies used in oncology trials, including Electronic Data Capture (EDC) systems and Good Clinical Practice (GCP) guidelines. Regulatory compliance is a key focus, with detailed lessons on MHRA and EMA regulations, informed consent, and Investigational Medicinal Product (IMP) regulations. The statistical aspects of clinical trials are also explored, with an emphasis on sample size calculation, data interpretation, and how to analyze clinical trial results effectively.

The course then examines the operations of clinical trials, focusing on site selection, monitoring, and adverse event reporting. Patient-centric approaches, including engagement, diversity, and retention strategies, are also covered to ensure clinical trials are inclusive and patient-focused. Practical case studies and group discussions offer real-world insights, allowing students to apply their knowledge to actual trial scenarios.

Emerging trends such as adaptive trial designs, personalized medicine, and innovations in oncology research are explored, along with the regulatory submission process and international collaboration in global trials. The course concludes with a recap of key takeaways, final project presentations, and an opportunity to earn certification upon successful completion.