Supply Chain Analyst

CY Partners
Ware, Hertfordshire
12 months ago
Applications closed

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Posted
20 Aug 2025 (12 months ago)

Supply Chain Analyst - Clinical Trials

Location: Ware

Contract Type: 12 Month Contract

Working Pattern: Hybrid - 2 days on site, 3 days WFH

Salary: Up to £21.05 p/h 

We’re seeking a detail-oriented and proactive Supply Chain Analyst to support key pre-production and temperature excursion management activities within Global Packaging Operations and Clinical Interface teams. This is an exciting opportunity to play a critical role in the timely delivery of clinical supplies to patients across the globe.

Key Responsibilities:

Execute and manage pre-production tasks to enable on-time handover of packaging jobs.

Approve GMP Manufacturing Requests (MRs) in local inventory systems for internal and external packaging activities.

Accurately complete documentation with a focus on quality and right-first-time principles.

Manage and document clinical site temperature excursions, in-transit excursions, and depot excursions to ensure uninterrupted clinical supply.

Conduct Veeva system activities to support clinical study leads and maintain the integrity of clinical trial information.

Participate in management monitoring activities, supporting audit readiness and quality compliance.

Collaborate with aligned Supply Chain Planners and Study Leads to maintain demand plans in local MRP systems (e.g., Supply Management Tool).

Manage inventory across the network to ensure correct stock placement and timely disposal of expired materials.

Own the post-packaging assessment and release process for new countries joining clinical studies.

Qualifications & Experience:

University degree or equivalent experience in a relevant discipline.

Proficient in Microsoft Office applications, particularly Excel, Word, and Outlook.

Solid understanding of GMPs and clinical packaging/manufacturing processes.

Experience working with document/quality management systems is desirable.

Ability to accurately review and approve documentation with strong attention to detail.

Self-motivated and capable of independently managing workload and priorities.

If this role sounds interesting to you apply now with a copy of your CV

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