Clinical Trial Supply Specialist
You will support our activities for drug supply in preclinical and clinical trials.
You will be responsible for designing Investigational Medicinal Product (IMP) supply strategies, and overseeing and coordinating execution. Tasks include authoring of trial related CMC documents.
The following qualifications are required:
Experience with clinical trial supply planning and delivery
Solid knowledge in GCP and GMP
You should be well organized, skilled in coordinating multiple stakeholders and work with a focus on quality. A good knowledge of English is required.
If you are interested in this position, please forward your resume along with a letter of motivation to:
Christine Frei, Human Resources
Neurimmune AG, Wagistrasse 13, CH-8952 Schlieren