Global Clinical Supply Chain Lead

Ipsen

England

Vor Ort

GBP 60.000 - 90.000

Vollzeit

Vor 9 Tagen

Eine vollständige Bewerbung in einer Minute

Maßgeschneiderter Lebenslauf und Anschreiben – versandbereit.

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Zusammenfassung

Ipsen is seeking a Clinical Supply Chain Project Manager to define IMP design and the associated supply chain strategy for clinical trials. You will coordinate with stakeholders to set up and maintain supply chain activities, including external CDMO management for outsourced projects, ensuring alignment with trial milestones and regulatory expectations.

Must have 3–5 years in pharma, strong project management, and experience with global clinical supplies.

Qualifikationen

  • 3–5 years of experience in the pharmaceutical industry with international exposure.
  • Experience managing complex investigational supplies for global clinical trials is required.
  • Strong project management skills and ability to facilitate cross-functional collaboration.

Aufgaben

  • Facilitate a cross functional CSC sub team for study setup, packaging, and distribution.
  • Represent GCSM in study team meetings and align with milestones and forecasts.
  • Define project objectives and develop comprehensive plans to ensure on-time supply to patients and avoid stockouts.
  • Collaborate with Regulatory and CMC teams to align regulatory strategy and submissions.
  • Monitor changes to scope, schedule and costs; provide mitigation and escalation as needed.
  • Present progress and results at internal and external meetings.

Kenntnisse

Project management
Stakeholder alignment
English proficiency

Ausbildung

Bachelor’s degree

Tools

RTSM platforms
Excel

Jobbeschreibung

Ipsen is seeking a Clinical Supply Chain Project Manager to define IMP design and the associated supply chain strategy for clinical trials. You will coordinate with stakeholders to set up and maintain supply chain activities, including external CDMO management for outsourced projects, ensuring alignment with trial milestones and regulatory expectations.

Must have 3–5 years in pharma, strong project management, and experience with global clinical supplies.

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