At a Glance
- Tasks: Shape clinical supply strategies and support global studies to deliver medicines to patients.
- Company: Join a passionate team dedicated to transforming lives through science.
- Benefits: Competitive pay, remote work, and a culture of innovation and inclusion.
- Other info: Dynamic role with opportunities for growth and meaningful contributions.
- Why this job: Make a real impact in the pharmaceutical industry while collaborating with diverse teams.
- Qualifications: Experience in clinical supplies or global supply chain, strong analytical skills required.
The predicted salary is between 51750 - 63250 £ per year.
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.
Clinical Trial Supplies Manager employer: Atrium
Atrium is an excellent employer that fosters a collaborative and innovative work culture, making it an ideal place for a Global Labelling Specialist. Employees benefit from ongoing professional development opportunities and the chance to work on cutting-edge labelling projects in the UK, ensuring both personal growth and meaningful contributions to the industry. With a focus on compliance and teamwork, Atrium provides a supportive environment where your expertise in regulatory labelling can truly shine.
