At a Glance
- Tasks: Manage clinical trial supplies and ensure timely delivery of quality products for global studies.
- Company: Join a leading pharmaceutical company focused on innovative clinical solutions.
- Benefits: Competitive hourly rate, remote work flexibility, and opportunities for professional growth.
- Other info: Fully remote role with one day a month in Uxbridge, London.
- Why this job: Make a real impact in the pharmaceutical industry while working on global clinical trials.
- Qualifications: Experience in clinical supplies or development, strong analytical and project management skills.
The predicted salary is between 28.76 - 28.76 £ per hour.
Manager, Trial Supplies Management
Duration
24 months (12months + 12 months)
Location
Remote within the UK - 1 day a month in Uxbridge, London
Working hours
- 35 hours per week
- Onsite requirements
- Fully remote - MUST BE UK based
Engagement Type
Via PAYE
Hourly rate
£28.76 per hour
LEGAL RIGHT TO WORK
You must have the legal right to work in the UK. No sponsorship is available.
Atrium Global
This role is for a client of ours within the pharmaceutical industry.
Atrium Global is supporting them in identifying an experienced professional to manage clinical trial supplies across a global portfolio.
Job Overview
The Manager, Trial Supplies Management will create and maintain supply strategies for investigational products, ensuring alignment with scientific, regulatory and clinical development needs.
The role supports global studies by developing supply plans, forecasting, monitoring inventory, and coordinating with internal teams and external partners to ensure timely delivery of quality clinical supplies.
RESPONSIBILITIES
- Collaborate with internal Global Clinical Supply Chain teams and external stakeholders to meet study needs.
- Define, plan and communicate clinical supply strategies in support of global clinical trials.
- Support continuous improvement initiatives across the function.
- Influence clinical and development timelines, protocol design and country selection.
- Review draft clinical protocols and communicate timelines and supply strategies to teams.
- Develop study supply forecasts and monitor utilisation against expectations.
- Issue manufacturing, packaging and labelling requests in line with planning timelines and regulatory requirements.
- Monitor investigational product use dates, support extensions and coordinate related labelling.
- Ensure timely delivery of clinical supplies, considering regulatory and QP release needs.
- Participate in development and approval of IRT specifications and maintain supply strategies at depot and site level.
- Attend internal Clinical Supply and Study Team meetings, highlighting risks and mitigation strategies.
- Work with Strategic Sourcing to procure commercial drug aligned with study and country requirements.
- Manage supply and demand estimates for budget purposes and update forecasts as plans evolve.
- Act as the primary contact for clinical supplies across assigned studies.
- Support actions linked to change controls.
- Prepare documentation such as e TMF content, CSR appendices and batch listings for inspection readiness.
- Enter product complaints and deviations, working with Quality partners on investigations.
- Manage conflicts or issues with internal and external collaborators.
- Contribute to departmental procedural documentation.
- Undertake additional duties as assigned.
REQUIREMENTS
- Previous experience in the pharmaceutical industry.
- Experience in Clinical Supplies or Clinical Development with global exposure.
- Strong understanding of the global drug development process and regulatory requirements.
- Strong analytical, communication, negotiation and project management skills.
- Knowledge of forecasting, planning, manufacturing, packaging, labelling, IVRS, logistics, stability and quality processes.
- Understanding of import and export requirements.
- Proficiency with IVRS and CTMS systems.
- Strong industry technology knowledge.
- Ability to drive consensus and translate strategy into action.
- Demonstrated leadership, teamwork, conflict resolution and influencing capabilities.
- Experience coaching and mentoring is desirable.
Clinical Trial Supplies manager in Bournemouth employer: Atrium (EMEA)
Atrium (EMEA) is an excellent employer that fosters a collaborative and innovative work culture, making it an ideal place for Data Scientists to thrive. Located in the vibrant city of London, employees benefit from a dynamic environment that encourages professional growth through continuous learning opportunities and exposure to cutting-edge analytics projects. With a focus on data-driven decision-making, Atrium empowers its team members to make meaningful contributions while enjoying a supportive atmosphere.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Supplies manager in Bournemouth
✨Get Familiar with Temporary Roles in Pharma
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We think you need these skills to ace Clinical Trial Supplies manager in Bournemouth
Some tips for your application 🫡
Highlight Your Relevant Experience:In the pharmaceutical industry, it's crucial to showcase any relevant experience you have, whether it's internships, lab work, or coursework. Let’s emphasise your familiarity with drug development processes and any hands-on experience you've had with lab equipment or clinical trials in your CV.
Mention Certifications and Training:If you’ve got any certifications relevant to pharmaceuticals, like Good Clinical Practice (GCP) or a certification in pharmacovigilance, make sure to include them. These show your commitment to the field and can make a positive impact on your application for a temporary role at Atrium (EMEA).
Show Your Flexibility and Availability:Temporary positions often require immediate availability and flexibility in working hours. In your cover letter, make it clear when you can start and your ability to adapt to changing schedules, as this is key to a successful application.
Express Your Learning Goals:Since this is a temporary role, we suggest discussing what you hope to learn or gain from the experience at Atrium (EMEA). This not only shows your eagerness but also helps employers see you as someone who’s ready to make the most out of the opportunity.
How to prepare for a job interview at Atrium (EMEA)
✨Know Your Regulations
In the pharmaceutical industry, it’s crucial to understand key regulations like GMP (Good Manufacturing Practices) or GCP (Good Clinical Practices). Brush up on these standards and be ready to discuss how they influence your work approach during your interview with Atrium (EMEA).
✨Emphasise Adaptability
Since this is a temporary role, show that you're ready to hit the ground running. Share examples from your past experiences that demonstrate your ability to adapt quickly to new environments or changes, especially in a fast-paced setting like pharmaceuticals.
✨Highlight Relevant Skills and Tools
Whether it’s laboratory techniques or software like LabWare or SAS, make sure you can confidently talk about your technical skills. If you have experience with any specific tools used in previous roles, relate that directly to how it can help Atrium (EMEA) achieve its goals.
✨Prepare for Technical Questions
Be ready for technical questions related to drug development processes or quality assurance. We should expect scenarios where you might have to troubleshoot a problem or suggest improvements on a project—this shows your problem-solving capability in a temporary role.
