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For Companies At a Glance
- Tasks: Manage clinical supplies for global studies and collaborate with teams to optimise strategies.
- Company: Join a leading global firm dedicated to improving patient health and product development.
- Benefits: Enjoy remote work flexibility with occasional travel to the Uxbridge office.
- Why this job: Be part of a mission-driven company that prioritises patient care and innovation.
- Qualifications: Degree in a scientific field or equivalent experience in the pharmaceutical industry required.
- Other info: Must have the right to work in the UK and may require a DBS check.
The predicted salary is between 50000 - 60000 £ per year.
Overview
CK Group are recruiting for a Clinical Trial Supplies Manager to join a global pharmaceutical company on a contract basis for 6 months.
Salary: £28.76 ph. This role is inside IR35.
Role
- Collaborate with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers
- Proactively defines, plans, and communicates the clinical supply chain strategy in support of global clinical studies
- Responsible for identifying and supporting strategies for continuous improvement
- Ensures timely delivery of quality clinical supplies for all assigned compounds and protocols
- Participates in the development, review and approval of Interactive Response Technology (IRT) specifications. Develops investigation product distribution strategies and maintains distribution and supply strategies at depot and site level according to study
Your Background
- Previous working experience in Clinical Supplies
- Knowledge of global drug development process and global regulatory requirements
- Strong knowledge of Forecasting and Planning and proficient knowledge of related areas, i.e. Manufacturing, Packaging & Labelling, IVRS, Logistics, Quality, Stability, etc.
- Proficient knowledge of import/export requirements
- Ability to translate broad strategies into specific objectives and action plans
Company
Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise 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 role is home-based, with one or two trips to Uxbridge per month.
Apply
For more information, or to apply for this Clinical Trial Supplies Manager please contact the Key Accounts Team on 01438 870011 or email pharmacontracts@ckagroup.co.uk. Please quote reference 156 466.
It is essential that applicants hold entitlement to work in the UK.
Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
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CK Group: Clinical Trial Supplies Manager employer: Biotech 365
Contact Detail:
Biotech 365 Recruiting Team
StudySmarter Expert Advice 🤫
We think this is how you could land CK Group: 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 with them 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 trial supplies, such as IVRS and CTMS systems. Being knowledgeable about these tools will show that you're proactive and ready to hit the ground running.
We think you need these skills to ace CK Group: Clinical Trial Supplies Manager
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the responsibilities and requirements of the Clinical Trial Supplies Manager position. Tailor your application to highlight relevant experience and skills that align with the role.
Highlight Relevant Experience: Emphasise your previous working experience in the pharmaceutical industry, particularly in roles focused on Clinical Supplies or Development. Use specific examples to demonstrate your knowledge of GCSC processes and global drug development.
Showcase Your Skills: Make sure to mention your strong knowledge of IVRS and CTMS systems, as well as your understanding of global regulatory requirements. This will help you stand out as a candidate who meets the essential criteria.
Craft a Strong Cover Letter: Write a compelling cover letter that explains why you are interested in the position and how your background makes you a suitable candidate. Be sure to reference the job title and include the job reference number (134 171) in your correspondence.
How to prepare for a job interview at Biotech 365
✨Understand the Clinical Supply Chain
Make sure you have a solid grasp of the clinical supply chain processes. Be prepared to discuss how these processes impact global clinical studies and how you can contribute to optimising them.
✨Showcase Your Relevant 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 role.
✨Familiarise Yourself with Regulatory Requirements
Brush up on global regulatory requirements related to drug development. Demonstrating your knowledge in this area will show that you understand the complexities involved in clinical trials.
✨Prepare for Cross-Functional Discussions
Since the role involves collaborating with various teams, practice discussing how you would approach cross-functional meetings. Think about how you can effectively communicate strategies and influence timelines.
