Senior Director Clinical Trial Supply (m/f/x), Bern
Client: CSL
Location: Bern
Job Category: Other
Job Reference: 9b135202d537
Job Views: 3
Posted: 14.03.2025
Expiry Date: 28.04.2025
Job Description:
To strengthen our Supply Chain department in Europe, we currently hire a Senior Director Clinical Trial Supply (m/f/x) (R-229882). This is a senior leadership role within the CSL Enterprise Supply Chain and is responsible for the strategic leadership and delivery of all services within the scope outlined below, including continuous improvements. You will report into the Head of Global Supply Chain & External Supply Integration, and 7 Managers will report into you.
The Role
* Provide strategic leadership and deliver an efficient, cost-effective clinical trial supply chain for CSL's clinical programs.
* Responsible for planning and forecasting of drug product, placebo, and ancillaries 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 good clinical practices (GCP).
* Ensure on-time supply delivery to clinical sites and quality and integrity of supply in compliance with requirements and company standard operation procedures (SOPs).
* Accountable for maintaining CSL's interactive response technology (IRT) system to support clinical supply management activities for all studies.
* Responsible for contract negotiation and vendor management of clinical supply vendors to ensure performance relative to key performance indicators (KPIs).
* Work closely with Clinical R&D and other departments to ensure optimal use of systems and processes to support clinical trial supply chain.
* Responsible for CSL Behring, CSL Seqirus, and CSL Vifor's obligations as sponsor of our clinical studies in relation to IMP, ensuring processes and systems are in place for ICH GCP compliant supply and handling of IMP.
* 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 experience related to clinical or operational supply.
* 5+ years' experience in clinical drug supply in the pharmaceutical industry with global responsibility.
* Demonstrated leadership experience.
* Strong knowledge and experience in GCP/GMP principles and relevant international standards and regulatory requirements.
* Willing to travel approx. 20% of your time.
We are looking forward to your application. Please ensure to apply online with your CV and certifications as well as your salary expectation.
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