Director, Clinical Supply Chain (Biopharma)

Location: Based out of the San Francisco or Cambridge office, with occasional travel required.

Salary: $205,000–$235,000 annually, plus equity, bonus, and benefits.

Company

hirify.global is a clinical-stage biopharmaceutical company developing therapies for metastatic breast cancer, including palazestrant and OP-3136.

What you will do

• Lead end-to-end clinical supply chain strategy and execution for a global, late-stage clinical program.
• Develop demand forecasts, supply plans, inventory strategies, depot operations, and distribution plans based on enrollment, manufacturing, dosing, and study scenarios.
• Oversee CDMOs, manufacturers, logistics providers, packaging, labeling, shipping, customs, product accountability, returns, reconciliation, and study closeout.
• Lead IRT/RTSM supply strategy, setup, testing, implementation, change control, and ongoing performance.
• Plan contingencies for enrollment variability, manufacturing delays, comparator availability, shelf-life constraints, and distribution disruptions.
• Support NDA submissions, regulatory approval, commercial supply transition, inspection readiness, budgets, vendor spend, and cross-functional decision-making.

Requirements

• Bachelor’s degree in a scientific, engineering, supply chain, operations, or related discipline; an advanced degree is preferred.
• Late-phase clinical development and global clinical supply chain management experience, with deep knowledge of end-to-end clinical trial supply processes.
• 15+ years of biotechnology or pharmaceutical industry experience, including 8+ years in clinical supply chain management.
• Strong knowledge of GMP requirements, global regulations, IRT/RTSM, QMS, inventory management, forecasting, and planning tools.
• Experience with global clinical labels, shipping, customs, comparator or standard-of-care drug supply, and programs approaching NDA or marketing applications.
• 5+ years of people management experience, along with strong project management, leadership, communication, and risk mitigation skills.

Nice to have

• Oncology clinical trial experience.
• Advanced degree in a relevant discipline.
• Experience supporting commercial readiness and transition from clinical to commercial supply.

Culture & Benefits

• Equal opportunity workplace with an emphasis on diverse expertise and backgrounds.
• Open, flexible, and friendly work environment.
• Competitive compensation and benefits package.
• Equity and bonus opportunities.
• Opportunities to develop a long-term career in a growing oncology organization.