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- Aufgaben: Lead and optimize clinical trial supply chains for CSL's programs.
- Arbeitgeber: CSL is a global biotechnology leader focused on innovative medicines.
- Mitarbeitervorteile: Enjoy competitive salary, career growth opportunities, and a dynamic work environment.
- Warum dieser Job: Join a mission-driven team making a real impact in healthcare.
- Gewünschte Qualifikationen: 12+ years in pharma/clinical supply; leadership experience required.
- Andere Informationen: Willingness to travel 20% of the time is necessary.
Das voraussichtliche Gehalt liegt zwischen 90000 - 126000 € pro Jahr.
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Client:
CSL
Location:
Job Category:
Other
Job Reference:
3f790c85ee2b
Job Views:
15
Posted:
06.03.2025
Expiry Date:
20.04.2025
Job Description:
To strengthen our Supply Chain department in Europe, we currently hire a
Senior Director Clinical Trial Supply (m/w/x)
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.
- You will be responsible for planning and forecasting of drug product, placebo and ancilliaries volume requirements throughout clinical programs.
- You will 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).
- You will 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 are fulfilled and that processes and systems are in place, which ensure an 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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Senior Director Clinical Trial Supply (m/f/x), Bülach Arbeitgeber: TN Switzerland
Kontaktperson:
TN Switzerland HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Senior Director Clinical Trial Supply (m/f/x), Bülach
✨Tip Number 1
Make sure to highlight your leadership experience in your conversations. Since this role involves managing a team of 7 managers, showcasing your ability to lead and inspire teams will be crucial.
✨Tip Number 2
Familiarize yourself with CSL's clinical programs and their supply chain processes. Being knowledgeable about their specific needs and challenges will help you stand out during discussions.
✨Tip Number 3
Network with professionals in the pharmaceutical industry, especially those with experience in clinical trial supply. Building connections can provide valuable insights and potentially lead to referrals.
✨Tip Number 4
Prepare to discuss your experience with GCP/GMP principles in detail. This knowledge is essential for the role, and demonstrating your expertise will show that you're a strong candidate.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Senior Director Clinical Trial Supply (m/f/x), Bülach
Tipps für deine Bewerbung 🫡
Understand the Role: Take the time to thoroughly read the job description for the Senior Director Clinical Trial Supply position. Understand the key responsibilities and required skills, as this will help you tailor your application effectively.
Tailor Your CV: Customize your CV to highlight relevant experience in clinical trial supply and leadership roles. Emphasize your 12+ years of pharmaceutical or clinical experience and any specific achievements that align with the job requirements.
Craft a Compelling Cover Letter: Write a cover letter that addresses your motivation for applying and how your background fits the role. Mention your experience with GCP/GMP principles and your ability to drive continuous improvements in clinical drug supply.
Prepare for Salary Expectations: Be ready to state your salary expectations clearly in your application. Research industry standards for similar positions to ensure your expectations are realistic and competitive.
Wie du dich auf ein Vorstellungsgespräch bei TN Switzerland vorbereitest
✨Showcase Your Leadership Experience
As a Senior Director, you'll need to demonstrate your leadership skills. Prepare specific examples of how you've successfully led teams in the past, particularly in clinical supply or pharmaceutical settings.
✨Understand GCP and GMP Principles
Make sure you have a solid grasp of Good Clinical Practice (GCP) and Good Manufacturing Practice (GMP) principles. Be ready to discuss how you've applied these standards in your previous roles.
✨Discuss Strategic Planning Skills
Since the role involves planning and forecasting drug product requirements, be prepared to talk about your experience with strategic planning. Highlight any tools or methodologies you've used to ensure efficient supply chain management.
✨Prepare for Vendor Management Questions
Vendor management is a key part of this role. Think about your experiences negotiating contracts and managing vendor relationships, and be ready to share how you've ensured performance against KPIs.
