Senior Director Clinical Trial Supply (m/f/x)

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Senior Director Clinical Trial Supply (m/f/x), Marburg

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Client:

CSL

Location:

Marburg, Germany

Job Category:

Other

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EU work permit required:

Yes

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Job Reference:

85464fa466aa

Job Views:

4

Posted:

21.06.2025

Expiry Date:

05.08.2025

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Job Description:

To strengthen our Supply Chain department in Europe, we are hiring a

Senior Director Clinical Trial Supply (m/w/x)

R-229882

This senior leadership role within the CSL Enterprise Supply Chain involves strategic leadership and delivery of services within the scope outlined below, including continuous improvements. You will report to the Head of Global Supply Chain & External Supply Integration, with 7 Managers reporting to you.

The Role

• Provide strategic leadership and ensure an efficient, cost-effective clinical trial supply chain for CSL\’s clinical programs.
• Plan and forecast drug product, placebo, and ancillary volume requirements throughout clinical programs.
• Oversee supply-related processes at study sites, including product receipt, handling, storage, dispensing, drug accountability/labelling, return, and destruction, in compliance with GCP.
• Ensure on-time supply delivery to clinical sites, maintaining quality and integrity in line with SOPs.
• Maintain CSL\’s interactive response technology (IRT) system for clinical supply management activities.
• Manage contracts and vendors for clinical supply vendors, ensuring KPI performance.
• Collaborate with Clinical R&D and other departments to optimize systems and processes supporting the clinical trial supply chain.
• Ensure CSL Behring, CSL Seqirus, and CSL Vifor\’s obligations as study sponsors are fulfilled, with systems in place for GCP-compliant IMP handling.
• Drive continuous improvements in clinical drug supply.

Your Skills and Experience

• University degree (BSc, MSc, PhD) in life sciences, engineering, logistics, or equivalent experience.
• 12+ years\‘ pharmaceutical or clinical supply experience.
• 5+ years\‘ experience in clinical drug supply with global responsibility.
• Demonstrated leadership experience.
• Strong knowledge of GCP/GMP principles and international standards.
• Willingness to travel approximately 20% of the time.

We look forward to your application. Please apply online with your CV, certifications, and salary expectations.

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CSL employees working at least 30 hours/week are eligible for benefits from day 1, including healthcare, financial protection, and resources supporting wellbeing at every life stage.

CSL Behring develops high-quality medicines for rare and serious diseases, with treatments in immunology, hematology, cardiovascular and metabolic, respiratory, and transplant areas, available in over 100 countries.

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