Clinical Supply Coordinator | Koordinator (m/w/d) klinische Versorgung (1421)

Brüggen Engineering GmbH

Ludwigshafen am Rhein, Rheinland-Pfalz, Deutschland
Published Apr 30, 2026
Full-time
Permanent

Job Summary

As a Clinical Supply Coordinator, you will play a pivotal role in the organization and provision of clinical trial supplies for global studies within the pharmaceutical industry. Your day-to-day responsibilities involve supporting project managers, coordinating standardized activities for clinical trials, and managing the logistics of packaging and labeling trial materials. You will also oversee the shelf-life extension of supplies, ensure regulatory compliance by drafting and revising GMP/GCP-relevant standard operating procedures (SOPs), and develop innovative strategies to optimize supply processes. This position is ideal for a detail-oriented professional with a background in science or healthcare who thrives in a collaborative, international environment. You will be instrumental in ensuring that clinical supply chains are efficient, compliant, and effectively managed, directly contributing to the success of global pharmaceutical research and development projects.

Required Skills

Education

Completed degree in Natural Sciences, Healthcare, or a comparable qualification.

Experience

  • Professional experience in pharmaceutical development or within a GMP/GCP environment.
  • Demonstrated experience in project management and process coordination.
  • Experience in the planning and logistics of clinical trial materials.

Languages

German (Fluent)English (Fluent)

Additional

  • Permanent full-time position located in the Mannheim/Ludwigshafen area. Must have excellent written and verbal communication skills in both German and English.