Medical Oncology Registrar & Pharmaceutical Physician.
Dually trained in clinical practice and pharmaceutical strategy. My work synthesizes patient-facing AI, behavioural science, and health policy to design 21st-century cancer care systems.
My work synthesizes four distinct areas. Click a tile to jump to the relevant publications.
View All Publications on Google ScholarBenchmarking LLMs (Gemini) for safety, empathy, and hallucination in clinical settings.
Comparative analysis of FDA/EMA approvals and the impact of Brexit on UK oncology access.
Identifying barriers to clinical trial recruitment in ethnic minority groups.
Applied research in Haematology-Oncology, ECMO, and Thrombocytopenia.
Reflections on AI in healthcare, oncology policy, and the future of medicine.
Coming Soon
I'm working on articles about AI safety in oncology, health policy reform, and the physician-scientist journey.
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Experience in leveraging clinical data to influence national policy frameworks. I focus on ensuring national infrastructure is prepared for the next generation of screening and AI technologies.
Operational leadership in large-scale trials (80,000+ participants). Bridging commercial strategy and clinical reality to minimise burden and maximise uptake.
3 years as Portfolio Mentor at Start Codon. Evaluated startups on regulatory viability and clinical fit, not just technology.
Medical Oncology Registrar & Pharmaceutical Physician. I possess a rare "bilingual" ability to translate between clinical teams and commercial/policy stakeholders.
Expertise in designing studies that satisfy both regulatory requirements (MHRA/FDA) and payer requirements (NICE/HTA).
Building psychological safety in high-stakes environments to allow teams to challenge the status quo and solve complex patient problems.
Available for collaboration, advisory, and consulting.
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