Clinical Trial Supplies Manager
Clinical Trial Supplies Manager

Clinical Trial Supplies Manager

London Temporary Home office (partial)
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At a Glance

  • Tasks: Manage clinical supply chains for global studies and collaborate with teams to meet project needs.
  • 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 Β£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.

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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

Knowledge of Global Clinical Supply Chain processes
Strong understanding of clinical trial protocols
Experience with IVRS and CTMS systems
Project Management skills
Excellent communication skills
Ability to influence timelines and study design
Strategic planning and execution
Problem-solving skills
Attention to detail
Understanding of global regulatory requirements
Collaboration and teamwork
Continuous improvement mindset
Adaptability to changing environments
Scientific knowledge relevant to pharmaceuticals

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 how your background aligns with the role and express your enthusiasm for contributing to the company's mission of putting patients first.

Highlight Relevant Skills: In your application, clearly outline your skills related to clinical trial supply chain management, including your familiarity with IVRS and CTMS systems. Mention any strategies you've implemented for continuous improvement in previous roles.

Follow Application Instructions: Ensure you quote the job reference 134 171 in all correspondence and confirm your entitlement to work in the UK. Double-check that all required documents are included before submitting your application through our website.

How to prepare for a job interview at CK Group

✨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 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.

✨Prepare for Cross-Functional Discussions

Since the role involves collaborating with various teams, practice articulating your thoughts clearly and confidently. Think about how you can effectively communicate strategies and improvements during cross-functional meetings.

Clinical Trial Supplies Manager
CK Group
Location: London
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