Senior Clinical Supply Chain Manager

h3Senior Clinical Supply Chain Manager /h3pLondon, United Kingdom /ppBelgrade, Serbia /ppParis, France /ppLisbon, Portugal /ppBudapest, Hungary /ppBasel, Switzerland /ppPrague, Czech Republic /ppSofia, Bulgaria /ppMadrid, Spain /ppStockholm, Sweden /ppBucuresti, Romania /ppFull time /ppR /ppThe Senior Clinical Supply Chain Manager is responsible for leading the strategic planning, oversight, and delivery of a portfolio of clinical supply chain projects, ensuring the effective and timely provision of clinical trial supplies across global studies. This role plays a key part in driving operational excellence, supporting continuous improvement initiatives, and contributing to the ongoing evolution and optimisation of Clinical Trial Supplies processes, systems, and capabilities. /ph3Essential Functions /h3ulliInterpret clinical trial protocols to create and execute an effective clinical trial supply chain solution. /liliCreate master English label text in accordance with relevant regulatory framework (e.g. Annex 13). /liliCreate and maintain demand forecasts and packaging plans so that packed clinical supplies are readily available in accordance with the project requirements. /liliInitiate packaging campaigns with the assigned vendor and provide oversight to ensure on-time delivery. /liliSetup, monitor, and where necessary, update study assigned Interactive Response Technology (IRT) systems to ensure study inventory is effectively managed. /liliCreate an appropriate distribution plan and have oversight of the assigned vendor(s) executing it. /liliAbility to work independently and proactively to ensure that the supply of all trial materials is delivered to the right place at the right time. /liliProvide ongoing budget tracking activities so that projects are run efficiently and in accordance with client approved quotations. /liliMaintains 100% compliance on all assigned training and applies learnings to everyday practice. /liliRemain up to date in all GxP and regulatory requirements applicable to the role. /liliLeads client and vendor related meetings where necessary to discuss clinical supply chain topics or status updates. /liliCreates a Temperature Excursion management plan. /liliManages the review and assessment process of Temperature Excursions reported to the IQVIA Clinical Trial Supplies team. /liliConducts thorough and regular risk management assessments to ensure all risks are systematically reviewed and appropriate mitigations are executed. /liliSupport client bid defence meetings as required. /liliSupports the development and optimisation of the CTS department and processes. /li /ulh3Qualifications /h3pBachelor’s degree in Life Sciences, Supply Chain Management, Business, or a related discipline. /pulliAt least 5 years of experience in Clinical Supply Chain Management within the clinical trials industry. /liliHands-on experience with Interactive Response Technology (IRT) systems, including their use in clinical trial supply planning and management. /liliDemonstrated project management skills, with the ability to plan, coordinate, and deliver multiple priorities effectively. /liliProven ability to build and maintain strong working relationships with internal and external stakeholders. /liliStrong communication and interpersonal skills, with the ability to provide clear direction and influence outcomes. /liliEffective problem-solving skills, with a proactive and solution-oriented approach. /liliProficiency in Microsoft Office applications, including Word, Excel, and PowerPoint. /liliFluency in English, with excellent written and verbal communication skills. /li /ulpIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at /ppIQVIA is committed to integrity in our hiring process and maintains a zero tolerance policy for candidate fraud. All information and credentials submitted in your application must be truthful and complete. Any false statements, misrepresentations, or material omissions during the recruitment process will result in immediate disqualification of your application, or termination of employment if discovered later, in accordance with applicable law. We appreciate your honesty and professionalism. /ppIQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create connections that accelerate the development and commercialization of innovative medical treatments. Everything we do is part of a journey to improve patient outcomes and population health worldwide. /ppTo get there, we seek out diverse talent with curious minds and a relentless commitment to innovation and impact. No matter your role, everyone at IQVIA contributes to our shared goal of helping customers improve the lives of patients everywhere. Thank you for your interest in growing your career with us. /ppEEO Minorities/Females/Protected Veterans/Disabled /p #J-18808-Ljbffr