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(Senior) Clinical Trial Supply Manager(m/w/x)
Description
As a Senior Clinical Trial Supply Manager, you will play a crucial role in ensuring the timely supply of investigational medicinal products for clinical trials. Your day-to-day responsibilities will involve coordinating with various teams, managing logistics, and driving vendor performance to support seamless study execution.
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Requirements
- •Bachelor’s or Master’s degree in Supply Chain, Logistics, Life Sciences, or related discipline
- •8 – 12 years’ experience in clinical trial supply management, ideally in oncology or biologics
- •Proven experience managing CDMOs and logistics vendors
- •Strong knowledge of GxP, GDP, IRT, QP release, import/export, and cold-chain operations
- •Strong project-management, problem-solving, and stakeholder-communication skills
- •Hands-on, execution-focused mindset; comfortable working autonomously in a fast-paced biotech environment
- •Fluency in English; German a plus
Education
Work Experience
8 - 12 years
Tasks
- •Translate study requirements into operational supply and distribution plans
- •Manage demand and supply planning for continuous and compliant IMP availability
- •Oversee packaging, labeling, QP release, distribution, and returns/destruction activities
- •Act as IRT system owner for supply chain activities
- •Lead day-to-day CDMO project coordination and timeline tracking
- •Monitor packaging and labeling progress, batch documentation, and distribution
- •Manage distribution plans and logistics schedules, resolving issues promptly
- •Define, implement, and maintain SOPs and compliant processes
- •Drive vendor performance through structured governance and proactive communication
- •Coordinate IMP, QC/stability sample, and DS-DP transfers and imports worldwide
- •Serve as the point of contact for clinical-site shipment queries and troubleshooting
- •Ensure adherence to GDP and import/export requirements
- •Represent Supply in study, program, and vendor governance meetings
- •Align with TechOps, Clinical Operations, Regulatory, QA, and Finance on study execution
- •Track and report key supply metrics and identify process improvements
- •Manage storage and transport insurance coverage
- •Review, approve, and track supplier invoices to ensure budget adherence
- •Contribute to continuous improvement initiatives and support evolving priorities
Languages
English – Business Fluent
German – Basic
Benefits
Flexible Working
- •Flexibility
Competitive Pay
- •Ownership
Career Advancement
- •Professional growth
Informal Culture
- •Supportive culture
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(Senior) Clinical Trial Supply Manager(m/w/x)
The AI Job Search Engine
Description
As a Senior Clinical Trial Supply Manager, you will play a crucial role in ensuring the timely supply of investigational medicinal products for clinical trials. Your day-to-day responsibilities will involve coordinating with various teams, managing logistics, and driving vendor performance to support seamless study execution.
Let AI find the perfect jobs for you!
Upload your CV and Nejo AI will find matching job offers for you.
Requirements
- •Bachelor’s or Master’s degree in Supply Chain, Logistics, Life Sciences, or related discipline
- •8 – 12 years’ experience in clinical trial supply management, ideally in oncology or biologics
- •Proven experience managing CDMOs and logistics vendors
- •Strong knowledge of GxP, GDP, IRT, QP release, import/export, and cold-chain operations
- •Strong project-management, problem-solving, and stakeholder-communication skills
- •Hands-on, execution-focused mindset; comfortable working autonomously in a fast-paced biotech environment
- •Fluency in English; German a plus
Education
Work Experience
8 - 12 years
Tasks
- •Translate study requirements into operational supply and distribution plans
- •Manage demand and supply planning for continuous and compliant IMP availability
- •Oversee packaging, labeling, QP release, distribution, and returns/destruction activities
- •Act as IRT system owner for supply chain activities
- •Lead day-to-day CDMO project coordination and timeline tracking
- •Monitor packaging and labeling progress, batch documentation, and distribution
- •Manage distribution plans and logistics schedules, resolving issues promptly
- •Define, implement, and maintain SOPs and compliant processes
- •Drive vendor performance through structured governance and proactive communication
- •Coordinate IMP, QC/stability sample, and DS-DP transfers and imports worldwide
- •Serve as the point of contact for clinical-site shipment queries and troubleshooting
- •Ensure adherence to GDP and import/export requirements
- •Represent Supply in study, program, and vendor governance meetings
- •Align with TechOps, Clinical Operations, Regulatory, QA, and Finance on study execution
- •Track and report key supply metrics and identify process improvements
- •Manage storage and transport insurance coverage
- •Review, approve, and track supplier invoices to ensure budget adherence
- •Contribute to continuous improvement initiatives and support evolving priorities
Languages
English – Business Fluent
German – Basic
Benefits
Flexible Working
- •Flexibility
Competitive Pay
- •Ownership
Career Advancement
- •Professional growth
Informal Culture
- •Supportive culture
About the Company
CatalYm
Industry
Healthcare
Description
CatalYm is a biotech company developing innovative immunotherapies to transform cancer patients’ lives.
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