Company Overview:

Pharmaceutical manufacturer for small and large molecules. Mid-szie company environment, English speaking role.

The Role

- Manage clinical trial packaging and distribution projects, ensuring delivery to agreed timelines, budget, quality, and client expectations.

- Act as the primary client contact throughout the project lifecycle.

- Coordinate project set-up, documentation, packaging, labelling, and distribution activities.

- Oversee inventory management and ensure continuous product availability.

- Work with IRT/RTSM systems, logistics providers, and general depots to support worldwide clinical trial supply.

- Ensure compliance with GMP/GDP requirements, SOPs, and quality standards.

- Monitor project budgets, identify risks, and support mitigation activities.

- Drive continuous improvement across processes, systems, and documentation.

Requirements





- 5+ years' experience in clinical trial supply, pharmaceutical operations, project management, or a related regulated environment.

- Experience in clinical packaging, labelling, distribution, or pharmaceutical supply chains.

- Strong stakeholder, client, and vendor management skills.

- Knowledge of IRT/RTSM systems and GMP/GDP regulations is advantageous.

- Excellent organisational, communication, and project management skills with the ability to manage multiple priorities.

- Degree in Life Sciences, Pharmacy, Supply Chain, Engineering, Business, or a related discipline preferred. Project management certification (PMP, PRINCE2, or equivalent) is beneficial but not essential.

📌 Clinical Trial Supply Manager (Madrid)
🏢 Discover International
📍 Madrid