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Senior Director Clinical Trial Supply (m/f/x), Maidenhead
Client:
CSL Location:
Maidenhead Job Category:
Other EU work permit required:
Yes Job Reference:
3cb60142740f Job Views:
54 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
To strengthen our Supply Chain department in Europe, we currently hire a Senior Director Clinical Trial Supply (m/w/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 are fulfilled and that processes and systems are in place to ensure 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. CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
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Client:
CSL Location:
Maidenhead Job Category:
Other EU work permit required:
Yes Job Reference:
3cb60142740f Job Views:
54 Posted:
22.01.2025 Expiry Date:
08.03.2025 Job Description:
To strengthen our Supply Chain department in Europe, we currently hire a Senior Director Clinical Trial Supply (m/w/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 are fulfilled and that processes and systems are in place to ensure 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. CSL employees that work at least 30 hours per week are eligible for benefits effective day 1. We are committed to the wellbeing of our employees and their loved ones. CSL offers resources and benefits, from health care to financial protection, so you can focus on doing work that matters. Our benefits are designed to support the needs of our employees at every stage of their life. CSL Behring is a global leader in developing and delivering high-quality medicines that treat people with rare and serious diseases. Our treatments offer promise for people in more than 100 countries living with conditions in the immunology, hematology, cardiovascular and metabolic, respiratory, and transplant therapeutic areas.
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