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Director, Clinical Supply Chain

Job in Northern, Floyd County, Kentucky, USA
Listing for: Blonde Inc.
Full Time, Part Time position
Listed on 2026-09-20
Job specializations:
  • Management
    Healthcare Management
Salary/Wage Range or Industry Benchmark: 180000 - 240000 USD Yearly USD 180000.00 240000.00 YEAR
Job Description & How to Apply Below

Location
:
Cambridge, MA (hybrid working with 2-3 days/week onsite)

Reporting to
:
Head of Supply Chain

About Hemab

Hemab is building preventative treatments for serious, underserved bleeding disorders. These are therapies designed to work with the body's own biology and stop bleeds before they start, instead of treating them after they happen. We're patient-first, science-led and clinical-stage - with a pipeline that takes different scientific approaches to different patient needs.

We went public via our 2026 IPO, and we're scaling across two homes:
Cambridge, MA, USA, and Copenhagen, Denmark.

The role

As Director, Clinical Supply Chain, you will lead the planning and execution of clinical supply activities across Hemab's development pipeline. Working across CMC and Manufacturing, Clinical Operations, Quality, Regulatory and other functions, you'll build and run the clinical supply capabilities needed to support programs across multiple modalities and geographies.

What you'll do
  • Develop and implement Clinical Supply Chain strategies to support the clinical program - ensure timely completion of all functional deliverables including applicable quality and regulatory documents.
  • Working with cross-functional teams (including R&D, Clinical Operations, Manufacturing, Quality, Regulatory, Legal and Finance), develop and implement compliant, robust, fit-for-purpose and cost-effective processes for Clinical Supply Chain in multiple geographies - with direct responsibility over multiple products for various modalities, and execute on them.
  • Be the lead to identify, select and manage vendors, suppliers, logistics partners for Clinical Supply Chain activities in collaboration with the other CMC and Manufacturing representatives to ensure continuum especially with DP, in support of future and ongoing clinical programs.
  • Lead, manage, supervise and coordinate the work of Clinical Supply Chain suppliers, consultants, vendors and collaborators as applicable to meet the programs goals.
  • Responsibility for all Clinical Supply Chain activities, in collaboration with Quality, for overall compliance with global distribution regulations ensuring that all vendors use systems and processes in compliance with all relevant regulatory standards. If needed represent the company as the Clinical Supply Chain expert in interactions with global health authorities.
  • Represent Clinical Supply Chain in one or more supply sub teams and actively contribute to define the clinical supply plans with her/his CMC and Manufacturing colleagues, in alignment with the other relevant functions like Clinical Operations.
  • Maintain state-of-the-art knowledge of Clinical Supply Chain providing guidance and advice to the executive team shaping product development and promoting use of latest technologies.
  • Maintain and enhance a network of consultants, vendors, suppliers and logistics partners to supplement internal capabilities, to adequately support active and future development programs.
  • Monitor and analyze Clinical Supply Chain performance metrics and implement improvements. Optimize inventory management to minimize costs and maximize efficiency.
  • Contribute to building a world class CMC and Manufacturing team for all Clinical Supply Chain related activities.
  • Formulate, monitor and control budgets for the Clinical Supply Chain part of the CMC and Manufacturing activities.
What you'll bring to Hemab
  • Educated at Bachelor’s degree level
  • Proven track record of extensive industrial experience in Clinical Supply Chain management - preferable in the biotech or pharmaceutical industry.
  • Demonstrable experience of working “hands-on” in building and managing clinical supply chain operations (including experience across US, EU and global clinical programs)
  • Prior working…
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