CRO/CDMO Study Management

Full study planning and management for in vitro, in vivo, and analytical programs, including protocol design, vendor oversight, assay development, data interpretation, and reporting. I work closely with internal teams and external CROs and CDMOs to ensure studies are clearly scoped, scientifically rigorous, and aligned with development objectives.

This includes translating program goals into executable study plans, monitoring study progress, addressing technical issues as they arise, and ensuring data quality throughout the process. By integrating data interpretation and reporting into the study lifecycle, I help teams generate decision-quality data that supports program advancement, risk reduction, and effective communication with stakeholders.

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