Executive Director, Clinical Supply Management

🏢 Jadebiosciences · 📍 Boston; Remote; San Francisco; Seattle; Vancouver · 💼 remote 💰 $280,000 - $300,000 / yr

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Position Summary & Responsibilities

About Jade Biosciences

Jade Biosciences is a clinical-stage biotechnology company focused on developing best-in-class therapies that address critical unmet needs in autoimmune diseases. Jade’s lead candidate, JADE101, targets the cytokine APRIL, and is currently being evaluated for the treatment of immunoglobulin A nephropathy. Jade’s pipeline also includes JADE201, an afucosylated anti-BAFF-R monoclonal antibody, as well as JADE301, an anti-IFN-β monoclonal antibody. Jade was launched based on assets licensed from Paragon Therapeutics, an antibody discovery engine founded by Fairmount. For more information, visit JadeBiosciences.com and follow the Company on LinkedIn.

Role Overview

Jade is developing potentially transformational, disease-modifying therapies for people living with autoimmune diseases. With three biologics programs in the clinic and multiple ongoing studies from Phase I to Phase III, we are seeking an experienced Executive Director, Clinical Supply Management to join our CMC leadership team and make sure every patient in our trials receives the right investigational product, on time.

Reporting to the Chief Technology Officer (Head of CMC), you will own clinical supply strategy, planning and execution for all Jade programs. You will shape and scale the Clinical Supply Management function, growing and mentoring a team of internal employees and contractors, and you will lead a global network of CMOs and logistics partners supporting complex, multi-country and multi-site studies with ambitious timelines and enrollment targets.

This is a high-impact role for a

🎯 Candidate Preparation Guide For Jadebiosciences Applicants

Key Role Competencies & Evaluation Highlights

Key Role Focus:

Assessment centers on translational scientific rigor, cross-functional biotech execution speed, and strategic target validation.

📋 Preparation Priorities (Key Areas to Clarify):

1. Showing attachment to a scientific hypothesis in the face of contradictory empirical data.
2. Operating in academic isolation without regard for biotech capital efficiency and timelines.
3. Weak grasp of regulatory pathways and preclinical translational milestones.

✨ Recommended Role Alignment Hook:

I accelerate biotherapeutic pipelines by aligning rigorous translational science with aggressive, milestone-driven drug development execution.

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