Job Description
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To strengthen our supply chain operations, we are seeking a seasoned professional to lead the strategic planning and execution of clinical trial supply chains. This role requires a strong understanding of pharmaceutical regulations, logistics, and leadership skills.
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The Role
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* Develop and implement efficient clinical trial supply chains to support CSL's global clinical programs.
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* Forecast and manage drug product, placebo, and ancillary volume requirements for clinical trials.
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* Oversee supply-related processes at study sites, ensuring compliance with good clinical practices (GCP) and company standard operating procedures (SOPs).
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* Maintain high-quality supply delivery to clinical sites and ensure integrity of supply in accordance with regulatory requirements.
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* Accountable for maintaining CSL's interactive response technology (IRT) system to support clinical supply management activities.
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* Negotiate contracts with clinical supply vendors to ensure performance relative to key performance indicators (KPIs).
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* Collaborate with Clinical R&D and other departments to optimize use of systems and processes supporting clinical trial supply chains.
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Your Skills and Experience
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* University degree in life sciences, engineering, logistics, or equivalent experience.
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* At least 12 years' experience in pharmaceutical or clinical roles related to clinical or operational supply.
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* 5+ years' experience in clinical drug supply with global responsibility.
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* Demonstrated leadership experience.
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* Strong knowledge of GCP/GMP principles and relevant international standards and regulatory requirements.
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* Fluent English skills.
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* Will to travel approximately 20% of working time.