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(Senior) Clinical Trial Supply Manager(m/w/x)
Managing IMP supply and distribution for oncology/biologics at an immunotherapy biotech, overseeing packaging, QP release, and IRT system ownership. 8-12 years clinical trial supply experience, with CDMO management, required. Flexible work options.
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
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
Work Experience
- 8 - 12 years
Education
- Bachelor's degreeOR
- Master's degree
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)
Managing IMP supply and distribution for oncology/biologics at an immunotherapy biotech, overseeing packaging, QP release, and IRT system ownership. 8-12 years clinical trial supply experience, with CDMO management, required. Flexible work options.
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
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
Work Experience
- 8 - 12 years
Education
- Bachelor's degreeOR
- Master's degree
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.
Not a perfect match?
- BioNTech SE
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Full-timeOn-siteSeniorMainz, München - ITM Isotope Technologies Munich SE
Legal Counsel Life Sciences(m/w/x)
Full-timeOn-siteSeniorGarching bei München - Futrue
Team Lead/Director Clinical Operations(m/w/x)
Full-timeOn-siteManagementGräfelfing - Coriolis Pharma Research GmbH
Laboratory Technical Services Lead(m/w/x)
Full-timeOn-siteSeniorPlanegg - LivaNova Deutschland GmbH
Team Lead Tactical Purchasing(m/w/x)
Full-timeOn-siteSeniorMünchen