CK Group: Clinical Trial Supplies Manager

Biotech 365; Uxbridge; Hybrid; GBP 80,000 - 100,000; Full time

Job summary

A leading global pharmaceutical company is seeking a Clinical Trial Supplies Manager for a 6-month contract role. This position involves collaboration across various teams to ensure optimal supply chain strategies for clinical studies. Ideal candidates will possess relevant scientific education, experience in the pharmaceutical industry, and knowledge of global drug development processes.

Qualifications

• Previous experience in the pharmaceutical industry.
• Experience focused on Clinical Supplies/Development with global experience.
• Strong understanding of global regulatory requirements.

Responsibilities

• Collaborates with internal and external teams to meet needs in clinical supply chain.
• Defines and communicates clinical supply chain strategy.
• Responsible for identifying and supporting strategies for continuous improvement.

Skills

Knowledge of GCSC processes

Strong knowledge of global drug development

Knowledge of IVRS and CTMS systems

Education

Degree in a relevant scientific subject or equivalent experience

Job description

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.


Please note:

This role may be subject to a satisfactory basic Disclosure and Barring Service (DBS) check.

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