Clinical Trial Supplies Manager

CK Group; London; Hybrid; GBP 50,000 - 60,000; Full time

Job summary

A global pharmaceutical company is looking for a Clinical Trial Supplies Manager to join their team on a 6-month contract basis. The role involves collaborating with various teams to communicate and implement clinical supply strategies and ensure optimal support for global clinical studies. The successful candidate will manage timelines, contribute to study designs, and drive continuous improvements in supply processes. This remote role involves occasional travel to the Uxbridge office.

Qualifications

• Previous working experience in the pharmaceutical industry is necessary.
• Prior experience in Clinical Supplies/Development with global experience is required.

Responsibilities

• Collaborates to ensure all needs are met for clinical supply chain.
• Defines and communicates clinical supply chain strategy in support of studies.
• Responsible for identifying strategies for continuous improvement.

Skills

Knowledge of GCSC processes

Understanding of global drug development process

Knowledge of IVRS and CTMS systems

Education

Degree in a relevant scientific subject

Job description

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CK Group are recruiting for a Clinical Trial Supplies Manager, to join a global pharmaceutical company, on a contract basis, for 6 months initially.

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.