Support of planning, set-up, conduct and close-out of (international) clinical trials Phase I-IV related to clinical trial monitoring
Monitoring oversight for (international) clinical trials
Co-Monitoring of clinical trial sites (including site...
Design study documents, including protocols, consent forms, clinical site agreements, ethics committee applications, etc.
Prepare clinical evaluation reports, develop partnerships with Clinical Research Organizations (CRO)
Working closely with...
For our Performance Polyamides production unit in Freiburg, where we focus on the polymerisation of Polyamide 66 and Copolyamide 66/6 under the brand name Stabamid, we are looking for a Process Engineer (m/f) to sustain the recognized roll of the...
Administrative support of the planning, set-up, conduct and close-out of international clinical trials Phase I-IV
Supporting the preparation of clinical trial related documents, especially specific forms and documents related to...
Independent development and optimization of cell-based and other bioanalytical assays with hands-on work in the lab
Transfer of methods to quality control department
Preparation of SOPs, reports and presentations...
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