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Contract

Supply Chain Analyst

Ware
money-bag Negotiable
Posted 3 days 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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