Would you like to play a key role in ensuring clinical supplies to clinical studies worldwide?

On behalf of a leading global pharmaceutical company, we are seeking a highly motivated and detail-oriented Clinical Supply Manager to join an international and innovative organization dedicated to developing advanced pharmaceutical products for oncology and diagnostic imaging.

This position offers the opportunity to take responsibility in complex end-to-end clinical supply chains supporting global clinical studies. The successful candidate will be responsible for establishing, planning, coordinating, and executing clinical supply activities to ensure investigational medicinal products (IMPs) and imaging products are available at clinical sites in the right quantity, at the right time, and in full compliance with applicable to quality and regulatory requirements. Furthermore, perform supply performance, inventory levels of a commercial product based on demand forecasts.

Key Responsibilities

· Develop and maintain clinical supply strategies and plans aligned with clinical study protocols and enrollment forecasts.
· Manage ordering, manufacturing coordination, materials, packaging, labeling, distribution, and inventory management of IMPs and imaging products.
· Establish and implement clinical supply operations for new countries, depots, and clinical study sites.
· Coordinate activities with Clinical Operations, Quality Assurance, Regulatory Affairs, CMC, external depots, and Contract Manufacturing Organizations (CMOs).

Provide oversight and support for supply and material-related activities connected to commercial product
· Monitor supply performance, inventory levels, demand forecasts, and key performance indicators.
· Identify supply chain risks and implement mitigation plans to ensure uninterrupted supply.
· Drive continuous improvement initiatives across clinical supply processes and systems by implementing IRT systems, AI tools and digital solutions.
· Ensure compliance with GMP, GDP, GCP, and applicable regulatory requirements.
· Maintain compliant supply documentation, procedures, and quality records.
· Support deviations, investigations, and change control activities.

Qualifications and Experience

· Bachelor's or Master's degree in Pharmacy, Life Sciences, Supply Chain Management, Logisticics, Engineering, or related disciplines.
· Relevant experience in clinical supply, pharmaceutical supply chain operations, logistics, manufacturing support, or related pharmaceutical functions.
· Strong understanding of Clinical Supply Chain Management and complex end-to-end supply chains.
· Knowledge of Investigational Medicinal Products (IMPs), imaging products, and clinical trial supply processes.
· Good understanding of GDP requirements and applicable regulatory frameworks.
· Knowledge of GMP, GCP, IRT systems and AI and digital tools, and quality management processes is advantageous.

Personal Attributes

· Highly organized with exceptional attention to detail.
· Strong analytical and problem-solving skills.
· Excellent communication and stakeholder management capabilities.
· Ability to work effectively across functions, cultures, and geographical regions.
· Comfortable operating in a fast-paced and time-sensitive environment.
· Proactive, accountable, and operationally focused.

What We Offer

· A central role within a globally recognized pharmaceutical company.
· Opportunity to contribute to innovative medicines and clinical development programs.
· Exposure to complex international clinical supply operations.
· A professional, collaborative, and highly competent working environment.
· Competitive compensation and attractive employment conditions.

About the Company

Our client is a globally recognized pharmaceutical company operating at the forefront of innovation, research, and development. The company's identity will be disclosed to selected candidates at an appropriate stage of the recruitment process.

If you are motivated by managing complex end-to-end clinical supply chains and ensuring the successful delivery of pharmaceutical products to clinical trial sites around the world, we look forward to receiving your application.

For further information, please contact Annemieke Nesse at Randstad tlf: 92209871 / annemieke.nesse@randstad.no. Applications will be handled with strict confidentiality.