Clinical Supply Chain Manager

JR United Kingdom; Stoke-on-Trent; On-site; GBP 45,000 - 65,000; Full time

Job summary

A leading life sciences recruiter is looking for a Clinical Supply Chain Manager in Stoke-on-Trent. This role involves managing the distribution of clinical trial supplies and ensuring timely delivery, compliance, and coordination with stakeholders. Ideal candidates will have strong logistics experience and knowledge of pharmaceutical standards.

Qualifications

• Experience in pharmaceutical supply chain management, particularly in clinical trials.
• Strong understanding of GXP, GCP, GDP, and GMP standards required.

Responsibilities

• Manage clinical demand and coordinate supply sourcing.
• Oversee project schedules ensuring alignment with clinical site demands.
• Address quality issues and monitor budgets.

Skills

Logistics planning

Communication

Problem-solving

Organizational skills

Stakeholder management

Flexibility

Adaptability

Tools

MS Office

ERP systems

Job description

Social network you want to login/join with:

Clinical Supply Chain Manager, Stoke-on-Trent

Client:

Proclinical Staffing

Location:

Stoke-on-Trent, United Kingdom

Job Category:

Other

EU work permit required: Yes

Job Views:

3

Posted:

04.06.2025

Expiry Date:

19.07.2025

Job Description:

Are you ready to drive the future of Clinical Supply Chain from behind the scenes? Looking to be in the heart of a company where precision meets purpose?

Proclinical is seeking a Clinical Supply Chain Manager to oversee the management and distribution of clinical trial supplies. This role involves coordinating supply chain activities to ensure timely delivery and compliance with regulatory standards. You will work closely with internal and external stakeholders to manage project schedules and supply needs.

Responsibilities:

• Manage clinical demand and coordinate with manufacturing for supply sourcing and lead times.
• Collaborate with clinical managers to determine investigational medicinal product (IMP) needs.
• Oversee project schedules and deliverables, ensuring alignment with clinical site demands.
• Serve as the primary contact for project challenges related to clinical trial supplies.
• Ensure timely project delivery through effective task coordination.
• Develop site-specific strategies for supply destruction/returns and maintain essential records.
• Monitor inventory levels and facilitate site-to-site transfers as needed.
• Notify relevant parties of any deviations affecting product quality.
• Contribute to SOP development and implement procedures for clinical trial demand.
• Establish communication pathways to support supply chain strategy development.
• Evaluate information to create a robust supply chain strategy minimizing waste.
• Lead coordination of activities with other business units and third parties.
• Oversee Interactive Response Technology (IRT) System setup for medication management.
• Perform risk assessments and monitor budgets to ensure project alignment with quotations.
• Address quality issues and temperature excursions promptly.

Key Skills and Requirements:

• Strong logistics planning experience.
• Proficiency in MS Office and ERP systems.
• Experience in pharmaceutical supply chain management, particularly in clinical trials.
• Understanding of GXP, GCP, GDP, and GMP standards.
• Effective communication and stakeholder management skills.
• Ability to define, report, and address business KPIs.
• Problem-solving, organizational, and decision-making skills.
• Flexibility and adaptability in a fast-paced environment.

If you are having difficulty in applying or if you have any questions, please contact Ed Little at [emailprotected].

If you are interested in applying to this exciting opportunity, then please click 'Apply' or request a callback at the top of this page to speak with one of our specialists.

Proclinical is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. Proclinical is acting as an Employment Agency in relation to this vacancy.

By submitting this application, you confirm that you've read and understood our privacy policy, which informs you how we process and safeguard your data - https://www.proclinical.com/privacy-policy.