Senior Clinical Supply Chain Manager
New
I
IQVIAClinical supply chain
Source API remote eligibility restrictions: United KingdomFull-TimeSenior
Salary not disclosed
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Job Details
- Languages
- Professional proficiency in English.
- Experience
- 3-5 Years industry experience in Clinical Trials (Essential); 3-5 Years experience in Clinical Supply Chain Management (Essential)
- Required Skills
- SAPMicrosoft Excel
Requirements
- Bachelor's degree in Life Sciences, Pharmacy, Supply Chain Management, Business, or a related discipline.
- 3–5 years of industry experience in clinical trials.
- 3–5 years of experience in clinical supply chain management.
- Strong understanding of clinical trial supply planning, demand forecasting, inventory management, packaging, labelling, distribution, and logistics.
- Experience with IRT/RTSM systems and clinical supply technologies.
- Knowledge of GCP, GMP, GDP, GxP, and applicable global clinical supply regulations.
- Project leadership and stakeholder management experience in matrixed global organisations.
- Ability to manage multiple studies, priorities, and external service providers simultaneously.
- Experience with complex supply planning across multiple studies, products, regions, or development programs.
- Experience with ERP systems, preferably SAP.
- Advanced Microsoft Office skills, particularly Excel and PowerPoint.
- Professional proficiency in English.
Responsibilities
- Interpret clinical trial protocols to create and execute clinical trial supply chain solutions.
- Create master English label text in accordance with applicable regulatory frameworks, such as Annex 13.
- Create and maintain demand forecasts and packaging plans to ensure clinical supplies are available according to project requirements.
- Initiate packaging campaigns with assigned vendors and oversee on-time delivery.
- Set up, monitor, and update study-assigned IRT systems to manage study inventory.
- Create distribution plans and oversee vendors executing them.
- Track project budgets and manage temperature excursion plans and assessments.
- Conduct risk assessments, lead client and vendor meetings, and support bid defence meetings.
- Support development and optimisation of clinical trial supplies department processes.
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