Global Clinical Supply Lead (Hybrid)

Witzig The Office Company AG

Allschwil

Hybrid

CHF 120.000 - 150.000

Vollzeit

14 Tage+
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Benefits dieser Stelle

Competitive salary

Zusammenfassung

Witzig The Office Company AG is seeking a Clinical Supply Manager in Allschwil, Basel-Landschaft. The role focuses on end‑to‑end management and timely delivery of trial supplies for global studies, coordinating with GMP/GCP teams and external vendors.

You will forecast demand, develop supply plans, manage inventory and packaging, and ensure regulatory compliance across sites. A hybrid work option with two days home office is available for a motivated biotech professional.

Qualifikationen

  • 3–5 years of experience in supply chain/logistics in clinical trials.
  • Extensive experience in project management and leadership in clinical supply.
  • GMP/GCP regulations and related requirements.
  • Experience with IRT and EDC systems (e.g. Medidata).
  • Ability to manage multiple studies in a fast-paced biotech setting.

Aufgaben

  • IMP and ancillary supply management for global trials.
  • Develop demand forecasts and supply plans based on protocols and enrollment.
  • Plan and execute supply strategy for trial medication and ancillaries with teams.
  • Oversee packaging, blinding setups, and distribution strategies.
  • Manage inventory, expiry, and re-supply with CMC collaboration.
  • Lead vendor selection, quotes, and communications with external vendors.
  • Monitor labeling/packaging, QA deviations, and SOP alignment.
  • Coordinate translations and local label texts, and master label text approval.
  • Report progress to line manager and manage project timelines.

Kenntnisse

Supply chain management
Project management
GMP/GCP knowledge
IRT/EDC systems
Leadership
Biotech environment

Tools

Medidata

Jobbeschreibung

Witzig The Office Company AG is seeking a Clinical Supply Manager in Allschwil, Basel-Landschaft. The role focuses on end‑to‑end management and timely delivery of trial supplies for global studies, coordinating with GMP/GCP teams and external vendors.

You will forecast demand, develop supply plans, manage inventory and packaging, and ensure regulatory compliance across sites. A hybrid work option with two days home office is available for a motivated biotech professional.

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