Speaker Information
Meet the speaker and learn more about their expertise, experience, and contribution to advancing clinical research.
Zubin Thacker
Director, Regulatory Affairs,
IQVIA
Zubin has over 19 years of experience in the pharmaceutical industry, with expertise in global and regional regulatory operations, compliance, and strategic leadership. He is responsible for implementing business strategy across multiple regions, ensuring regulatory compliance, overseeing the training and development of regulatory professionals, and supporting the development of systems and processes to meet evolving regulatory requirements.
Zubin serves as an industry representative for ACRO on the EMA ACT EU Advisory Group. He represents IQVIA in trade association forums and acts as a trusted advisor to both IQVIA and regulatory authorities, providing strategic insight on clinical trial regulatory policy, compliance, and operational best practices.
