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Supply Chain Manager for Clinical Trial medications

Supply Chain Manager for Clinical Trial medications

Reference: BBBH28984
Date posted: 09/04/2026
Job details
Specialism
Technical Operations
Expertise
Quality Control
Location
Gothenburg, Sweden
Job type
Contract
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Description

Drive the end‑to‑end supply chain that delivers critical clinical trial medications to patients worldwide.

R&D Partners is seeking a Supply Chain Manager to oversee clinical trial medication logistics in a fast-paced R&D environment. This role is pivotal in ensuring the availability of high-quality clinical trial supplies for patients worldwide.

Please note that to be considered for this role you must have the right to work in this location.

Responsibilities:

  • Project Management: Design, plan, and set up study supply chains to ensure timely delivery of clinical supplies.
  • Cross-Functional Collaboration: Lead teams and maintain continuous dialogue with internal and external partners to address study design requirements and changes impacting supply chain elements.
  • Risk Management: Proactively identify and mitigate risks affecting supply quality or delivery timelines.
  • Inventory Management: Handle inventory tasks such as rework, recalls, shelf-life extensions, expiry date management, and stock destruction.
  • IRT System Management: Execute demand and supply planning using Interactive Response Technology (IRT).
  • Quality Compliance: Operate within GMP Quality Management Systems, managing deviations, complaints, and change controls effectively.

Key Skills and Requirements:

Essential:

  • Bachelor’s degree in a scientific or business field (or equivalent experience).
  • Experience in supply chain environments or the pharmaceutical industry.
  • Holistic understanding of end-to-end supply chain activities.
  • Expertise in demand planning, forecasting, and risk identification/management.
  • Strong project management skills with the ability to influence customer demands.
  • Excellent English communication skills (written and verbal).
  • Proficient IT skills and adaptability to bespoke systems.
  • Ability to learn and evolve with new processes and transformations.

Desirable:

  • Awareness of GMP (Good Manufacturing Practice) and GCP (Good Clinical Practice).
  • Knowledge of clinical development processes related to clinical material supply.
  • Lean methodology knowledge.
  • Experience handling quality events, deviations, change controls, and complaints.

For more information, please contact Grant Van Schalkwyk.

If you are interested in applying to this exciting opportunity, then please click ‘Apply’ or to speak to one of our specialists visit the ‘Contact Us’ page.

R&D Partners is a leading life sciences recruiter focused on finding exceptional people and matching them with the finest positions across the globe. R&D Partners 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.r-dpartners.com/privacy-policy/

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Register your interest

If you can’t find your ideal role with us right now, we’d still love to hear from you! Send us your CV and we’ll contact you if a suitable role becomes available.

Register interest

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