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Sap s/4hana data design specialist

Bedford
Jr United Kingdom
Design
Posted: 27 August
Offer description

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Client:

Insight Global


Location:

bedford, United Kingdom


Job Category:

Other

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EU work permit required:

Yes

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Job Views:

1


Posted:

26.08.2025


Expiry Date:

10.10.2025

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Job Description:

Insight Global are looking to hire a SAP S/4Hana Data Design specialist to lead the design of supply chain and clinical data objects. The role will support transformation efforts and stakeholder engagement across global teams for a global SAP S/4HANA transformation programme.

Please note, this role is for a multi year 12-month contract (Outside IR35), based 3 days a week onsite in either Luton or Macclesfield, 2 days remote.

Key Responsibilities Include:

* Design and maintain data models for clinical supply chain objects, including investigational product inventory, shipment tracking, and trial site logistics.
* Collaborate with clinical operations, supply chain, and IT teams to ensure data structures support end-to-end clinical supply processes.
* Lead change management initiatives to embed new data designs and processes across global teams.
* Manage cross-functional teams and coordinate with stakeholders to deliver scalable and compliant data solutions.
* Ensure data integrity, consistency, and compliance with GxP and regulatory standards.
* Utilize SAP (ideally S/4HANA) to support data design, integration, and reporting across clinical supply systems.

Must-haves:

* Proven experience in data design within clinical supply chain or life sciences environments.
* Strong change and engagement skills
* Proven task, team, and stakeholder management
* SAP and S/4HANA proficiency
* Strong understanding of SAP systems, especially S/4HANA, and their application in clinical supply management.
* Excellent team leadership and task management capabilities.
* Familiarity with regulatory requirements and data governance in clinical trials.

Plusses:

* Degree in Life Sciences, Supply Chain, Data Management, or a related field.
* Experience in GxP-regulated environments and clinical trial logistics.
* Certification in SAP or data architecture frameworks.
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