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Responsible for all aspects of site management and monitoring activities for assigned applicable phase I and phase II-IV clinical investigator sites within the approved Clinical Development Plan (CDP)
Manage investigator site, site activities and...
Support our research projects with cell culture expertise, including preparation of scientific proposals for our customers
Presentation of projects to other project managers as well as to our external partners
Design and development of...
the Associate Director Quality CSV (Computerized System Validation) is responsible to define the Quality IT validation strategy for the deployment and maintenance of Electronic Quality Systems for GMP/GDP related activities of Merck Biopharma...
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