Clinical Research Associate con 2 años de experiencia en industria (CRO o farma). Experiencia en cualquier area terapeutica sera valorada.
- NonStop Consulting - Alicante, Alicante provincia
- NonStop Consulting - León, León provincia
Work in accordance with GMP regulations. Report the work done and the needs of the Microbiological Quality Control department to the person in charge of the…
- NonStop Consulting - Madrid, Madrid provincia
My client who is a mid-size CRO is currently looking for a Regulatory Medical Writer to join their team Fully Remotely, Anywhere in Europe on a permanent basis!