Clinical Trial Supplies Manager

TN United Kingdom; London; Remote; GBP 100,000 - 125,000; Full time

Job summary

A global pharmaceutical company is seeking a Clinical Trial Supplies Manager for a 6-month contract. The role involves collaborating with teams to ensure clinical supply chain needs are met, influencing timelines, and supporting continuous improvement strategies. The position requires a degree in a scientific field and experience in the pharmaceutical industry. This role is primarily remote with occasional travel to the Uxbridge office.

Qualifications

• Previous experience in the pharmaceutical industry.
• Experience in Clinical Supplies/Development with global exposure.

Responsibilities

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

Skills

Knowledge of GCSC processes

Proficiency with IVRS and CTMS systems

Education

Degree in a relevant scientific subject

Job description

Job Title: Clinical Trial Supplies Manager

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

Salary: Up to £30.03 per hour PAYE

Role and Responsibilities:

1. Collaborate with internal Global Clinical Supply Chain (GCSC) teams, external customers, and service providers to ensure all needs are met.
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, communicate timelines, and investigational product strategies.

Qualifications and Experience:

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

Company Overview:

Our client is a global leader in 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:

This role is remote with travel to the Uxbridge office 1-2 times a month.