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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 innovative drug development.
- Qualifications: Degree in a scientific field or equivalent experience in the pharmaceutical industry required.
- Other info: Applicants must have the right to work in the UK and may need a DBS check.
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
Network with professionals in the pharmaceutical industry, especially those who have experience in clinical trial supplies. Attend relevant webinars or industry events to make connections and learn more about the role.
✨Tip Number 2
Familiarise yourself with the latest trends and technologies in clinical supply chain management. Being knowledgeable about IVRS and CTMS systems will give you an edge during discussions with potential employers.
✨Tip Number 3
Prepare to discuss your previous experiences in detail, particularly any roles that involved collaboration with global teams. Highlight specific examples where you influenced timelines or contributed to study design.
✨Tip Number 4
Research the company’s mission and values, especially their focus on patient care. Be ready to articulate how your personal values align with theirs during interviews, as cultural fit is often a key consideration.
We think you need these skills to ace Clinical Trial Supplies Manager
Some tips for your application 🫡
Understand the Role: Read the job description carefully to understand the key responsibilities and requirements for the Clinical Trial Supplies Manager position. Tailor your application to highlight relevant experience and skills that align with these expectations.
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 global drug development processes and regulatory requirements.
Showcase Your Skills: Make sure to showcase your strong knowledge of IVRS and CTMS systems. Mention any relevant tools or software you have used in past roles that would be beneficial for this position.
Craft a Strong Cover Letter: Write a compelling cover letter that not only summarises your qualifications but also expresses your enthusiasm for the role and the company. Mention how your values align with their goal of putting patients first and improving lives.
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.
✨Prepare for Cross-Functional Discussions
Since the role involves collaborating with various teams, practice discussing complex topics clearly and concisely. Think about how you can effectively communicate strategies and improvements during cross-functional meetings.
✨Understand Regulatory Requirements
Brush up on global regulatory requirements related to drug development. Being able to discuss these regulations confidently will demonstrate your expertise and readiness for the role.
