Clinical Trial Supplies Manager

CK Group- Science, Clinical and Technical; City Of London; Remote; GBP 80,000 - 100,000; Full time

Job summary

A leading global pharmaceutical company is looking for a Clinical Trial Supplies Manager to manage clinical supply chains for global studies. You will collaborate with teams to deliver quality supplies and improve strategies. Candidates should have prior experience in Clinical Supplies and an understanding of regulatory processes. The position is home-based with occasional trips to Uxbridge.

Qualifications

• Must have previous experience in Clinical Supplies.
• Strong understanding of global regulatory requirements.
• Proficiency in areas such as Manufacturing, Packaging, Logistics, and Quality.

Responsibilities

• Collaborate with internal teams and external service providers.
• Define and communicate clinical supply chain strategy.
• Ensure timely delivery of quality clinical supplies.

Skills

Previous working experience in Clinical Supplies

Knowledge of global drug development process

Strong knowledge of forecasting and planning

Proficient knowledge of import/export requirements

Ability to translate broad strategies into specific objectives

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.

Salary: £28.76 ph. This role is inside IR35.

Clinical Trial Supplies Manager Role

• Collaborate with internal Global Clinical Supply Chain (GCSC) teams and external Customers and Service Providers.
• Proactively define, plan, and communicate the clinical supply chain strategy in support of global clinical studies.
• Identify and support strategies for continuous improvement.
• Ensure timely delivery of quality clinical supplies for all assigned compounds and protocols.
• Participate in the development, review, and approval of Interactive Response Technology (IRT) specifications.
• Develop investigation product distribution strategies and maintain distribution and supply strategies at depot and site level according to study.

Your Background

• Previous working experience in Clinical Supplies.
• Knowledge of global drug development process and global regulatory requirements.
• Strong knowledge of forecasting and planning, and proficient knowledge of related areas such as Manufacturing, Packaging & Labelling, IVRS, Logistics, Quality, Stability, etc.
• Proficient knowledge of import/export requirements.
• Ability to translate broad strategies into specific objectives and action plans.

Company

Our client is the global leader in enabling pharma, biotech, and consumer health partners to optimise product development, launch, and full life-cycle supply for patients around the world. They aim to put patients first and help people everywhere live better and healthier lives.

Location

This role is home‑based, with one or two trips to Uxbridge per month.

Apply

For more information, or to apply for this Clinical Trial Supplies Manager, please contact the Key Accounts Team. Please quote reference (Apply online only).

It is essential that applicants hold entitlement to work in the UK.

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

INDKA