Senior Clinical Supplies Project Manager

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

💊 Pharmaceuticals

🧬 Biotechnology

⚕ Healthcare Insurance

Pharmaceuticals ‱ Biotechnology ‱ Healthcare Insurance

ICON plc is a global provider of clinical, consulting, and commercial services across various sectors in the healthcare and pharmaceutical industries. They offer a wide range of clinical solutions, including decentralised clinical trials, cardiac safety solutions, early clinical laboratories, and medical imaging. ICON also provides technology solutions that support drug development from early phases to post-marketing. Their therapeutic expertise spans cardiovascular, oncology, internal medicine, and more, with a strong focus on transformative therapies like cell and gene therapies and biosimilars. ICON is recognized as a leading Contract Research Organisation (CRO), regularly providing thought leadership and contributing to industry publications and events. Their services are tailored to optimize clinical trials, offer regulatory intelligence, and deliver real-world evidence through robust data analysis and patient-centric solutions.

📋 Description

‱ Leading the planning, execution, and management of clinical supplies projects, including timelines, budgets, and resource allocation. ‱ Collaborating with cross-functional teams to develop supply strategies that align with study requirements and regulatory guidelines. ‱ Overseeing supplier relationships, negotiating contracts, and ensuring high-quality and timely delivery of clinical supplies. ‱ Monitoring project progress and performance metrics, identifying risks, and implementing mitigation strategies as necessary. ‱ Providing leadership and guidance on best practices in clinical supply management and project execution.

🎯 Requirements

‱ Bachelor's degree in supply chain management, logistics, life sciences, or a related discipline ‱ Extensive experience in clinical supplies management or project management, preferably within the pharmaceutical or biotechnology industry. ‱ Strong understanding of clinical trial processes and regulatory requirements related to clinical supplies. ‱ Excellent organizational and problem-solving skills, with the ability to manage multiple projects simultaneously. ‱ Strong communication and interpersonal skills, with the ability to collaborate effectively with diverse teams and stakeholders.

đŸ–ïž Benefits

‱ Competitive base salary and performance related incentives ‱ Health and wellbeing programmes including medical, dental, and vision coverage where applicable ‱ Retirement and pension plans ‱ Life assurance and disability coverage ‱ Employee assistance programmes and wellbeing resources ‱ Learning and development opportunities through structured training and career pathways

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