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Director, Clinical Supply
Job in
Burlington, Middlesex County, Massachusetts, 01805, USA
Listed on 2026-08-30
Listing for:
Scorpion Therapeutics
Full Time
position Listed on 2026-08-30
Job specializations:
-
Supply Chain/Logistics
Supply Chain & Logistics, Logistics Coordination, Inventory Control & Analysis, Procurement / Purchasing
Job Description & How to Apply Below
Key Responsibilities:
- Develop and execute clinical supply strategies aligned with development timelines and program goals.
- Execute clinical supply chain activities including labeling, packaging, distribution, inventory management, forecasting, initiation, maintenance, and expiry of clinical supplies.
- Lead commercial supply readiness activities: supply planning, inventory strategy, distribution readiness, and cross-functional coordination for product launch/commercialization.
- Manage relationships with external partners (CDMOs, CROs, logistics providers) to ensure timely, efficient, and compliant delivery.
- Lead clinical supply planning and risk mitigation to prevent disruptions.
- Liaise with stakeholders to support timely approval and execution of SOPs, batch records, lot releases, change controls, deviations, and CAPAs.
- Ensure compliance with global regulatory requirements, GMP standards, and internal quality systems.
- Collaborate with Clinical Operations, Regulatory Affairs, Quality Assurance, and CMC teams.
- Monitor inventory levels and implement proactive supply chain solutions.
- Contribute to vendor selection, contract negotiations, and budget management.
- Other responsibilities as assigned.
Qualifications:
- Bachelor’s or Master’s in a scientific discipline with 12+ years of relevant experience in clinical supply chain and logistics.
- Hands-on experience managing labeling, packaging, distribution, inventory management, forecasting, and IRT initiation, maintenance, and expiry.
- Experience managing clinical supply vendors and contract manufacturers.
- Strong operational skills tracking multiple activities, deliverables, timelines, contracts, and budgets.
- In-depth knowledge of quality and regulatory aspects for multi-country clinical studies (biologics/peptides).
- Excellent problem-solving, strategic thinking, and ability to work in a fast-paced, collaborative environment.
- Strong scientific leadership, collaboration, interpersonal skills, self-awareness, and ability to manage team dynamics.
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