Clinical Trial Supply Coordinator | Coordinator (m/w/d) Clinical Trial Supply
Merck KGaA
Job Summary
Join a dynamic Healthcare team as a Clinical Trial Supply Coordinator, where you'll play a pivotal role in optimizing clinical trial processes. You will support the Operational Excellence Team by coordinating projects aimed at developing, improving, and harmonizing processes with both internal and external stakeholders. A key part of your day-to-day will involve developing and implementing Standard Operating Procedures (SOPs) and collaborating closely with Quality Assurance and Qualified Persons on release-relevant documentation. You'll also be responsible for reviewing and archiving technical specifications and contracts, overseeing outsourced study activities, and meticulously documenting business activities. This role is ideal for someone passionate about ensuring GMP compliance for drug supply, returns, and destructions, ensuring timely delivery and storage of medications, and contributing to the advancement of healthcare.
Required Skills
Education
Completed training in pharmaceutical-technical or commercial fields, or a degree in natural science-pharmaceutical or commercial fields.
Experience
- Long-term specific professional experience in pharmaceutical-technical or commercial fields, or relevant studies in natural science-pharmaceutical or commercial fields
- Knowledge of the pharmaceutical industry, especially regarding clinical trial execution, logistics, manufacturing, or quality assurance
- Knowledge of international requirements (GMP, GDP, and GCP rules) for medicinal products and investigational medicinal products
- Professional experience in clinical trial management and monitoring (advantageous)
Languages
Additional
- This is a fixed-term position for two years.
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