CK Group: Clinical Trial Supplies Manager

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

Job summary

A global pharmaceutical company is seeking a Clinical Trial Supplies Manager for a 6-month contract. This remote role involves collaboration with clinical supply teams and requires a degree in a scientific field. The ideal candidate will have experience in the pharmaceutical sector and strong knowledge of drug development processes. Applicants should be prepared for occasional travel to the Uxbridge office.

Qualifications

• Previous experience in the pharmaceutical industry, particularly in Clinical Supplies.
• Experience with global exposure in drug development.

Responsibilities

• Collaborate with internal teams and external customers to meet needs.
• Define and communicate clinical supply chain strategy.
• Influence clinical and development timelines.

Skills

Knowledge of GCSC processes

Strong knowledge of global drug development

Education

Degree in a relevant scientific subject

Tools

IVRS

CTMS

Job description

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

Salary: Up to £30.03 per hour PAYE

Role Responsibilities:

1. Collaborate with internal Global Clinical Supply Chain (GCSC) teams, external customers, and service providers to meet all needs.
2. Define, plan, and communicate the clinical supply chain strategy to support global clinical studies.
3. Demonstrate strong knowledge of GCSC processes in cross-functional meetings.
4. Identify and support strategies for continuous improvement.
5. Influence clinical and development timelines, study design, and country selection.
6. Review and provide input to draft clinical protocols, communicating timelines and investigational product strategies.

Candidate Requirements:

• Degree in a relevant scientific subject or equivalent working experience.
• Previous experience in the pharmaceutical industry, particularly in Clinical Supplies/Development with global exposure.
• Strong knowledge of the global drug development process and regulatory requirements.
• Experience with IVRS and CTMS systems.

Company Overview:

Our client is a global leader enabling pharma, biotech, and consumer health partners to optimize product development, launch, and full lifecycle supply, aiming to put patients first and improve lives worldwide.

Location:

Remote role with travel to Uxbridge office 1-2 times a month.

Application Process:

For more information or to apply, contact the Key Accounts Team at 01438 870011 or email [e-mail]. Please quote reference 134171.

Applicants must have entitlement to work in the UK. Note: A satisfactory DBS check may be required.