Clinical Trial Supplies Manager

CK Group; United Kingdom; Remote; Full time

Job summary

CK Group is seeking a Clinical Trial Supplies Manager for a global pharmaceutical company on a 6-month contract. In this remote role, you'll manage clinical supply strategies and collaborate with teams to ensure effective drug development processes, requiring a degree and industry experience.

Qualifications

• Degree in a relevant scientific subject or equivalent experience.
• Previous experience in the pharmaceutical industry.
• Experience in Clinical Supplies/Development.

Responsibilities

• Collaborates with internal and external teams.
• Defines and communicates supply chain strategy.
• Responsible for identifying improvement strategies.

Skills

Strong knowledge of GCSC processes

Knowledge of IVRS

Knowledge of CTMS systems

Strong knowledge of drug development process

Education

Degree in a relevant scientific subject

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 GBP28.76 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 in all correspondence.

Please note:

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

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