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 in England 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.
StudySmarter Expert Advice🤫
We think this is how you could land Clinical Trial Supplies Manager in England
✨Get Familiar with Temporary Roles in Pharma
Temporary positions in the pharmaceutical industry often arise during specific periods, like product launches or seasonal hiring sprints. Keep an eye on timelines and be proactive in reaching out to companies, especially around these busy times!
✨Join Pharma Networking Events
Participate in local and virtual pharmaceutical networking events or job fairs. This is a fantastic way to get in front of hiring managers and learn more about temporary opportunities directly from those in the know.
✨Leverage Your University Career Services
If you’re a student or recent grad, tap into your university’s career services which often have specific connections to pharma companies looking to fill temporary roles. They might even have exclusive internship programmes that lead to temp jobs!
✨Be Visible Online and Offline
Utilise platforms like LinkedIn to share your interests in temporary roles and connect with industry professionals. Plus, consider writing about relevant pharmaceutical topics to showcase your knowledge and enthusiasm—this can help you stand out to hiring companies like Atrium.
We think you need these skills to ace Clinical Trial Supplies Manager in England
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.
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. 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
✨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.
✨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 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.
