Clinical Trial Supply Manager

Job not on LinkedIn

🕒 August 12

🌐 Bulgaria, Poland, +1 more countries – Remote

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⏰ Full Time

🟡 Mid-level

🟠 Senior

👔 Manager

đŸ‘» Ghost score 23%

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Logo of ICON plc

ICON plc

10,000+ employees

Founded 1990

đŸ’Œ Consulting

đŸ„ Healthcare

📩 Logistics

Consulting ‱ Healthcare ‱ Logistics

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

‱ Oversee the planning and execution of clinical supplies projects, ensuring timely delivery and compliance with regulatory requirements ‱ Collaborate with cross-functional teams to design and implement effective strategies for clinical trial supply management ‱ Monitor and analyze project timelines, budgets, and resource allocations to optimize efficiency and meet project goals ‱ Address potential risks and challenges in clinical supplies logistics, proposing and implementing solutions to ensure smooth project execution ‱ Foster strong relationships with internal and external stakeholders, facilitating effective communication and collaboration throughout the project lifecycle ‱ Oversee project and programme management workstreams, ensuring deliverables meet quality and timeline expectations ‱ Design and analyse clinical trials, interpreting complex medical data, and contribute to the advancement of innovative treatments and therapies

🎯 Requirements

‱ Bachelor's degree in a relevant field, such as pharmacy, life sciences, or supply chain management ‱ Proven experience in clinical supplies project management within the pharmaceutical or biotech industry ‱ Strong understanding of regulatory requirements related to clinical trial supply management ‱ Excellent organizational and communication skills, with the ability to guide cross-functional teams and drive project success ‱ Problem-solving mindset, with the ability to adapt to changing project dynamics and implement effective solutions ‱ Solid project and programme management experience ‱ Ability to manage competing priorities and develop your team ‱ Legal right to work in the country where the role is based

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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