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- Aufgaben: Lead the clinical trial supply chain and ensure efficient delivery of services.
- Arbeitgeber: Join CSL, a global leader in biopharmaceuticals dedicated to saving lives.
- Mitarbeitervorteile: Enjoy competitive salary, career growth opportunities, and a collaborative work environment.
- Warum dieser Job: Make a real impact in clinical trials while working with innovative teams.
- 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 72000 - 108000 € pro Jahr.
Social network you want to login/join with: Senior Director Clinical Trial Supply (m/f/x), St. Gallen Client: CSL Location: St. Gallen Job Category: Other Job Reference: 4c1ad3e70307 Job Views: 4 Posted: 03.03.2025 Expiry Date: 17.04.2025 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 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 and ensure processes and systems are in place that 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. #J-18808-Ljbffr
Senior Director Clinical Trial Supply (m/f/x), St. Gallen Arbeitgeber: Whatjobs
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Whatjobs HR Team
StudySmarter Bewerbungstipps 🤫
So bekommst du den Job: Senior Director Clinical Trial Supply (m/f/x), St. Gallen
✨Tip Number 1
Make sure to highlight your leadership experience in your conversations. As this role involves managing a team of 7 managers, demonstrating your ability to lead and inspire others will be crucial.
✨Tip Number 2
Familiarize yourself with CSL's current clinical programs and supply chain processes. Showing that you understand their specific needs and challenges can set you apart during interviews.
✨Tip Number 3
Network with professionals in the pharmaceutical industry, especially those with experience in clinical trial supply. This can provide you with valuable insights and potentially useful connections.
✨Tip Number 4
Prepare to discuss your experience with GCP/GMP principles in detail. Being able to articulate how you've applied these standards in past roles will demonstrate your expertise and readiness for this position.
Diese Fähigkeiten machen dich zur top Bewerber*in für die Stelle: Senior Director Clinical Trial Supply (m/f/x), St. Gallen
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 to highlight relevant experiences.
Highlight Relevant Experience: In your CV and cover letter, emphasize your 12+ years of pharmaceutical or clinical experience, particularly in clinical drug supply. Provide specific examples of your leadership roles and how you've successfully managed supply chains in previous positions.
Showcase Your Skills: Make sure to mention your strong knowledge of GCP/GMP principles and any relevant international standards. If you have experience with contract negotiation and vendor management, include that as well, as it is crucial for this role.
Prepare Your Application Documents: Ensure your CV is updated and includes all necessary certifications. Don't forget to include your salary expectations as requested in the job posting. A well-organized application will make a positive impression.
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✨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.
✨Prepare for Strategic Discussions
Since this role involves strategic leadership, think about how you would approach planning and forecasting drug product requirements. Be prepared to discuss your strategies and how they align with CSL's goals.
✨Familiarize Yourself with CSL's Operations
Research CSL's operations, especially their clinical programs and supply chain processes. Understanding their specific challenges and successes will help you tailor your responses and show your genuine interest in the company.
