Associate Director, Clinical Supply Management (UK/EU)

Location: Oxford, UK; Zug, Switzerland; or Dublin, Ireland

Salary: $83,000–$97,500 USD annually, with potential bonus, stock, benefits, and other variable compensation.

Company

hirify.global is a biopharmaceutical oncology company developing investigational therapies and conducting global Phase 3 clinical studies in lung and colorectal cancer.

What you will do

• Support the Senior Director in setting strategy, operating plans, budgets, governance, and performance objectives for global clinical supply management.
• Lead clinical supply execution across demand forecasting, supply planning, inventory, packaging, labelling, release, distribution, resupply, returns, reconciliation, and destruction.
• Act as a delegate in cross-functional governance forums, supplier reviews, issue escalations, and operational decision-making.
• Manage and develop direct reports by setting objectives, coaching performance, balancing workloads, and building team capability.
• Oversee CDMO, IXRS, and specialist service-provider relationships, including contracting support, implementation, performance management, and troubleshooting.
• Drive operational excellence through standardized processes, KPIs, dashboards, root-cause analysis, continuous improvement, and inspection readiness.

Requirements

• BSc, MSc, engineering, pharmacy, or equivalent degree, with at least 8 years of progressive supply chain experience in pharmaceutical, biotechnology, or CDMO environments.
• Experience leading complex international clinical studies and product supply chains, with knowledge of regulatory and GMP requirements for investigational and commercial products.
• Prior people-management experience, including objective setting, coaching, delegation, talent development, and performance management.
• Strong skills in clinical supply planning, forecasting, project and budget management, risk management, resource planning, supplier governance, and negotiation.
• Knowledge of IXRS design, setup, and UAT, as well as FDA, EMA, PMDA, GMP, GCP, Annex 13, SOPs, change controls, deviations, investigations, and CAPAs.
• Ability to work independently on complex global problems, influence cross-functional stakeholders, and operate as a trusted deputy to the Senior Director.

Culture & Benefits

• Work within a mission-driven oncology organization focused on improving quality of life and addressing serious unmet medical needs.
• Collaborate with global colleagues across Clinical Operations, Commercial, CMC, Quality, Regulatory, Finance, Legal, Procurement, Medical Affairs, and Program Management.
• Potential total compensation package including bonus, stock, benefits, and other variable compensation.
• Inclusive workplace built around integrity, excellence, purposeful urgency, collaboration, and commitment to people.