Speaker Information
Meet the speaker and learn more about their expertise, experience, and contribution to advancing clinical research.
Amber McNair
Associate Director of Clinical Trials Regulatory,
IQVIA Ltd
Amber McNair is Associate Director of Clinical Trials Regulatory at IQVIA, with over 15 years of combined experience in clinical laboratories and regulatory affairs. She specialises in biomarker driven clinical trials, IVD regulation, and integrated CTR/IVDR strategies, supporting sponsors in the development and execution of complex drug diagnostic programmes across Europe and globally.
Amber provides strategic leadership for global regulatory programmes involving personalised medicine and emerging diagnostic technologies. As an active contributor to industry discussions on IVDR implementation and combined drug diagnostic development, she works closely with sponsors and regulatory stakeholders to address the practical challenges of biomarker driven research in Europe.
