Clinical Supplies Chain Manager

JR 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 an initial 6-month contract. This largely remote role requires UK-based applicants due to contract status and onsite travel needs. The position involves managing clinical supply strategies, ensuring timely delivery, and liaising with vendors. The company focuses on innovation and cutting-edge techniques in their science.

Benefits

Holiday Pay

Pension

Qualifications

• Previous experience in a clinical development role within a pharmaceutical setting.
• Strong knowledge of clinical supply and drug development processes.

Responsibilities

• Manage clinical supply strategies within clinical studies.
• Create clinical development timelines and identify strategies for issues.
• Liaise with external vendors and services.

Skills

Communication

Analytical Skills

Tools

IRT

CTMS

Job description

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Our client, a global pharmaceutical company, is currently looking for a Clinical Trial Supplies Manager to join their team. This role is being offered on £28.50 per hour + holiday pay + pension for PAYE and £38.50 per hour (umbrella). Please note that no limited company contractors can be considered as the role is inside IR35.

Whilst this is largely remote requirement, only applicants living within the UK can be considered due to the contract status and due to the need to travel onsite.

This is a great opportunity to work for a pharmaceutical company on an initial 6-month contract who have created a centre of excellence and constantly focus on driving innovation and using cutting edge techniques in their science.

Key Responsibilities

• Manage clinical supply strategies within clinical studies whilst ensuring these delivered in a timely and cost-efficient manner
• Create clinical development timelines and proactively identify strategies and solutions for any issues that may arise
• Support the creation of medical protocols drafts and in the developing of package and label outlines
• Act as the clinical supplies point of contact and liaise with external vendors and services
• Ensure all products meet protocols and regulatory requirements

Requirements

• Previous experience in a clinical development role within a pharmaceutical setting
• Strong knowledge of clinical supply and drug development processes
• Understanding of global regulatory requirements
• Previous experience in planning and managing clinical studies strategies
• Good knowledge of IRT and CTMS systems
• Excellent communication and analytical skills

Park Street People Ltd is an Equal Opportunities Employer. We do not discriminate on the grounds of age, race, gender, disability, creed or sexual orientation and comply with all relevant UK legislation. We are acting as an Employment Business in relation to this role.