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- Tasks: Manage clinical supplies for global studies and collaborate with teams to optimise strategies.
- Company: Join a leading global pharmaceutical company dedicated to improving patient health worldwide.
- Benefits: Enjoy remote work flexibility with occasional travel to the Uxbridge office.
- Why this job: Be part of a mission-driven team that prioritises patient care and innovation in healthcare.
- Qualifications: Degree in a scientific field or equivalent experience in the pharmaceutical industry required.
- Other info: This role may require a basic DBS check; applicants must be eligible to work in the UK.
The predicted salary is between 50000 - 60000 £ per year.
CK Group are recruiting for a Clinical Trial Supplies Manager, to join a global pharmaceutical company, on a contract basis, for 6 months initially.
Salary: Up to £28.76 per hour PAYE.
Clinical Trial Supplies Manager Role:
- Collaborates with internal Global Clinical Supply Chain (GCSC) teams, external Customers & Service Providers Medical to ensure all needs are met.
- Defines, plans & communicates the clinical supply chain strategy in support of global clinical studies to promote optimal use.
- Demonstrates strong knowledge of GCSC processes when presenting at cross-functional meetings.
- Responsible for identifying and supporting strategies for continuous improvement.
- Influences clinical and development timelines, study design & country selection.
- Reviewing & providing input to draft clinical protocols, communicating timelines & investigational product strategies.
Your Background:
- Degree in a relevant scientific subject or have equivalent working experience.
- Previous working experience in the pharmaceutical industry.
- Prior experience in a role focussed on Clinical Supplies/Development with global experience or equivalent experience.
- Strong knowledge of the global drug development process & global regulatory requirements.
- Strong knowledge of IVRS and CTMS systems.
Company: Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full life-cycle supply for patients around the world. They have the goal of putting patients first and to help people around the world live better and healthier lives.
Location: This is a remote role with travel to the Uxbridge office, 1-2 times a month.
Apply: It is essential that applicants hold entitlement to work in the UK. Please quote job reference 134 171 in all correspondence. This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Clinical Trial Supplies Manager employer: New Scientist
Contact Detail:
New Scientist Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land Clinical Trial Supplies Manager
✨Tip Number 1
Familiarise yourself with the global drug development process and regulatory requirements. This knowledge will not only help you in interviews but also demonstrate your commitment to understanding the industry.
✨Tip Number 2
Network with professionals in the pharmaceutical industry, especially those who have experience in clinical supplies. Engaging in conversations can provide insights into the role and may even lead to referrals.
✨Tip Number 3
Prepare to discuss specific examples of how you've contributed to continuous improvement in previous roles. Highlighting your problem-solving skills will set you apart from other candidates.
✨Tip Number 4
Stay updated on the latest trends and technologies in clinical supply chain management. Being knowledgeable about IVRS and CTMS systems will show that you're proactive and ready to contribute from day one.
We think you need these skills to ace Clinical Trial Supplies Manager
Some tips for your application 🫡
Tailor Your CV: Make sure your CV highlights relevant experience in clinical supplies and the pharmaceutical industry. Emphasise any roles where you've collaborated with global teams or influenced clinical timelines.
Craft a Strong Cover Letter: In your cover letter, address how your background aligns with the job requirements. Mention your knowledge of GCSC processes and your ability to support continuous improvement strategies.
Highlight Relevant Skills: Clearly outline your understanding of IVRS and CTMS systems in your application. This is crucial for the role and will demonstrate your technical expertise.
Follow Application Instructions: Ensure you quote the job reference 134 171 in your application. This shows attention to detail and helps the hiring team track your application.
How to prepare for a job interview at New Scientist
✨Understand the Clinical Supply Chain
Make sure you have a solid grasp of the clinical supply chain processes. Be prepared to discuss how you would define and communicate strategies that support global clinical studies, as this will be crucial in your role.
✨Showcase Your Experience
Highlight your previous experience in the pharmaceutical industry, especially any roles focused on Clinical Supplies or Development. Be ready to provide specific examples of how your background aligns with the requirements of the position.
✨Familiarise Yourself with Regulatory Requirements
Demonstrate your knowledge of global regulatory requirements and the drug development process. This will show that you understand the complexities involved in clinical trials and can navigate them effectively.
✨Prepare for Cross-Functional Discussions
Since the role involves presenting at cross-functional meetings, practice articulating your thoughts clearly and confidently. Think about how you can influence timelines and study designs, and be ready to discuss these topics during the interview.
