Korro
Biopharmaceutical
AssociateDirector,ClinicalSupplyChainManagement
“Associate Director, Clinical Supply Chain Management at Korro. Skills: Clinical supply chain, Supply chain strategy, Vendor management, Regulatory compliance. Lead strategic and operational management. Develop and implement supply chain strategies”
What You'll Achieve.
Ensure uninterrupted, compliant, cost-effective delivery; Prevent stockouts
Industry & Context.
Identify risks; Implement solutions
Flexibility to travel on company business
What They're Looking For.
Must Have
Bachelor's or advanced degree, 10 years of relevant experience, Global clinical trial supply management, Labeling, packaging, distribution experience, IRT/IXRS inventory management, GMP and global regulations compliance, Global regulatory requirements understanding, External vendor selection and management, Global supply chain experience, Cold chain distribution experience, Logistics experience, Manage multiple projects, Identify risks and implement solutions, Excellent written & verbal communication, Work independently with minimal oversight, Interpersonal skills, Function in a dynamic team environment, Computer skills, Proficiency in spreadsheet software, Proficiency in presentation software, Proficiency in word processing software, Flexibility to travel
Nice to Have
Trade compliance experience, Import/exports/customs requirements experience
What You'll Do.
Lead strategic and operational management
Develop and implement supply chain strategies
Develop clinical forecasts/demand plans
Optimize supply chain operations
Establish and manage vendor relationships
Track invoices to contracts
Manage creation of label text/translation
Manage design of study drug packaging
Develop IRT supply & return strategy
Lead/oversee IRT set up
Participate in User Acceptance Testing
Develop requirements/specifications for clinical study drug
Ensure on time delivery of clinical supplies
Monitor IMP inventory levels
Coordinate resupply to prevent stockouts
Author study specific pharmacy manuals
Author supply related training/instructional materials
Oversee shipping & handling of temperature-sensitive products
Manage temperature excursions
Support investigations & CAPA
Collaborate with manufacturing sites & shipping companies
Develop & establish procedures/framework for global material movement
Collaborate with Quality Assurance & Regulatory
Support regulatory submissions
Ensure inspection readiness for global regulatory audits
Establish and maintain clinical supply & distribution SOPs
Support compliance and continuous improvement
Follow procedures for release of IMP
How You'll Work.
Team & Collaboration
Clinical Operations/Development; Quality; Regulatory Affairs; External partners; Manufacturing sites; Shipping companies; Quality Assurance; Regulatory
Communication Scope
Written communication; Oral communication
Process & Methodology
Manage multiple projects
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