Clinical Trial Supplies Manager
Remote
Contract -24 month
Pay rate: £28.76 p/h
Atrium is seeking a talented Clinical Trial Supplies Manager to help shape clinical supply strategies that support global clinical studies and deliver investigational medicines to patients.
Key responsibilities
• Partner with Global Clinical Supply Chain teams, clinical development, pharmaceutical development, quality, vendors and medical colleagues to support global study needs.
• Define, plan and communicate clinical supply chain strategies aligned to study and corporate objectives.
• Review clinical protocols, influence study design considerations and provide input on timelines, country requirements and investigational product strategy.
• Develop supply forecasts, monitor inventory and analyse drug utilisation against forecast, regulatory requirements and logistics timelines.
• Coordinate manufacturing, packaging and labelling requests to ensure investigational product supply aligns with protocol and regulatory needs.
• Support use-date extension activities, depot and site distribution strategies, IRT specifications and inspection readiness documentation.
• Manage supply risks, change controls, deviations, complaints and issue resolution in partnership with internal and external stakeholders.
• Act as the main clinical supplies contact for assigned compounds and studies, contributing to meetings and ensuring clear communication of supply strategy, risks and mitigation plans.
Experience required:
• Experience in the pharmaceutical industry, ideally within clinical supplies, clinical development or a global clinical supply chain environment.
• Strong understanding of the global drug development process, regulatory requirements and clinical study supply needs.
• Knowledge of forecasting, planning, manufacturing, packaging and labelling, logistics, quality, stability and import/export requirements.
• Experience working with IRT/IVRS and CTMS systems, with strong analytical and project management skills
• Ability to influence cross-functional teams, manage competing priorities and translate broad strategies into clear action plans.
• A collaborative, accountable and results-focused approach, with the ability to lead through ambiguity and build consensus.
Why to apply
You’ll be part of a passionate, inclusive culture focused on transforming patients’ lives through science. Sharing value of passion, innovation, urgency, accountability, inclusion and integrity help every colleague contribute to meaningful change.
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