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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 and competitive pay of up to £30.03 per hour.
- Why this job: Be part of a mission-driven team that prioritises patient care and innovative drug development.
- Qualifications: Degree in a scientific field or equivalent experience in the pharmaceutical industry required.
- Other info: Role involves occasional travel to Uxbridge; DBS check may be necessary.
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 £30.03 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 role is remote 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. Please note: This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.
Clinical Trial Supplies Manager employer: CK Group
Contact Detail:
CK Group 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 during discussions.
✨Tip Number 4
Stay updated on the latest trends and technologies in clinical trial management systems (CTMS) and interactive voice response systems (IVRS). Being knowledgeable about these tools will show your readiness for the role.
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 your knowledge of GCSC processes and any global experience you have.
Craft a Strong Cover Letter: Write a cover letter that specifically addresses the requirements mentioned in the job description. Discuss your background in clinical trial management and how it aligns with the company's goals of optimising product development.
Highlight Relevant Skills: In your application, clearly outline your skills related to IVRS and CTMS systems, as well as your understanding of global regulatory requirements. This will demonstrate your suitability for the role.
Follow Application Instructions: Ensure you quote the job reference 134 171 in your application. Double-check that you meet the entitlement to work in the UK and are prepared for a potential DBS check.
How to prepare for a job interview at CK Group
✨Know Your Clinical Supply Chain
Make sure you have a solid understanding of the global clinical supply chain processes. Be prepared to discuss how these processes impact clinical studies and how you can contribute to optimising them.
✨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 you've influenced timelines or study designs in past projects.
✨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 and can navigate them effectively.
✨Prepare for Cross-Functional Discussions
Since the role involves collaborating with various teams, practice discussing how you would communicate strategies and timelines in cross-functional meetings. Think about how you can influence and support continuous improvement initiatives.
