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Clinical Supply Associate

Göteborg, Sweden💼 Full-time🗓 2026-06-22 → 2026-06-28

Core

Support Clinical Supply Chain Management in delivering clinical material and associated information to meet agreed clinical demand.

Role type

Clinical Supply Associate

Builds

Clinical material and associated information for clinical trials

Domain

Pharmaceutical Technology and Development

Deliverable

client delivery

Required skills

Documentation, coordination, quality control, electronic Trial Master File management, inspection readiness, User Acceptance Testing, Supply Chain Management systems, visual management, problem solving, global standardisation, process confirmation

Preferred skills

Leadership skills, enterprise acumen

Technologies

Supply Chain Management systems, electronic Trial Master File

Responsibilities

Documentation and coordination of Product Quality Complaints, Coordination of Product Quality Sample Returns, Documentation and facilitation of Deviations affecting product quality or regulatory compliance, Management of documents in the electronic Trial Master File, Facilitation of documentation activities ensuring inspection readiness to meet international GMP standards, User Acceptance Testing, Continually improving Clinical Supply Chain processes

Seniority

Individual Contributor

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