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Preclinical and clinical formulation development
Validation of analytical methods and GLP/GMP manufacturing of drug products (oral and parenteral)
Writing SOPs and supporting QA colleagues from CMC perspectives
QPS Austria GmbH is an international successful full-service contract research organization (CRO) in the area of preclinical and clinical research. To cover monitoring activities in Germany we are searching for a homebased
Qualification and validation of external computerized systems used at medac in the area of clinical research (both on premise hosted systems and cloud-based systems)
Surveillance and monitoring of systems used by research organizations (CROs) on...
Working in the department for Clinical Development, the Clinical Trial Manager is responsible for the planning and implementation of all aspects of clinical trials, mainly relating to cellular therapies You will ensure that all...
Conducting and coordinating data management activities for clinical study projects
Supervision of trials and data management oversight in clinical trials outsourced to CROs
Supporting the clinical trial manager in a clinical trial by...
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