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Lead analytical development and QC for small molecule drug discovery and CMC activities. Define control strategies, develop and validate analytical methods, manage CDMO transfers, author regulatory CMC sections, maintain quality systems, oversee reference standards, and support cross-functional teams to enable GMP manufacture, release, and stability for clinical programs.

The Vice President of Program and Portfolio Management will lead the management of therapeutic programs from discovery to clinical development, ensuring strategic alignment and operational excellence across the organization.

The role involves providing strategic and operational leadership in GCP Quality Assurance for clinical studies and vendor programs, ensuring compliance and data integrity.

Lead end-to-end program management for preclinical through clinical development programs, owning integrated plans, timelines, risk mitigation, and governance. Align cross-functional stakeholders, prepare executive presentations, and drive decision-ready execution using program management tools and best practices to advance small-molecule drug candidates toward IND/CTA and clinical milestones.