David O’Connor is a seasoned clinical research professional with over 35 years of experience across clinical and pre‑clinical development, specializing in operational excellence, quality systems, and regulatory compliance within complex research environments.

Mr. O’Connor earned a Bachelor of Science with Honors in Chemistry from McGill University. His strong scientific foundation, combined with decades of hands‑on industry experience, has enabled him to work effectively across clinical, bioanalytical, and quality operations, fostering collaboration and driving sustainable compliance initiatives.

Throughout his career, Mr. O’Connor has held key leadership and consulting roles within Contract Research Organizations (CROs), a generic pharmaceutical manufacturer, and independent advisory settings. In these positions, he has successfully led multidisciplinary teams, guided operational improvements, and supported organizations through periods of growth and regulatory complexity.

His areas of expertise include data integrity assessments, preparation for and follow‑up to regulatory inspections, and the implementation of compliant processes that align quality objectives with business strategy. Mr. O’Connor is particularly valued for his ability to translate regulatory expectations into practical, scalable solutions that support both operational efficiency and inspection readiness.

Mr. O’Connor brings a pragmatic, collaborative approach to leadership and is committed to maintaining the highest standards of quality, integrity, and regulatory compliance. He and the team at Agassiz Clinical Research Partners look forward to partnering with sponsors to deliver reliable, high‑quality clinical research outcomes.