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Clinical Trial Planning and Conduct in Oncology: Fundamentals, Strategies and Best Practices
Oncology is the largest therapeutic area in drug development, accounting for nearly half of the biopharmaceutical industry’s $200 billion per year investment in R&D. Because oncology clinical development is exceptionally competitive, costly, and fast-paced, mastering its unique complexities is essential for success. Join us for this full day workshop intended to guide you through the fundamentals of oncology clinical trials—from initial strategic planning to final regulatory approval. This workshop is intended for professionals with little to no prior experience who seek to build or enhance collaborations with clinical development teams or transition into an oncology-focused career. Our speakers are seasoned experts from pharma and biotech companies who will describe core concepts and provide practical real-world examples to facilitate deep understanding.
Topics:
- Early and late clinical development strategies, study design, protocol development
- Patient safety, pharmacovigilance, and regulatory reporting requirements
- Biostatistics, biomarkers, and dose optimization
- Trial operations, data management, and quality assurance
- Regulatory considerations
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