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Provide appropriate clinical scientific input & support for all activities related to clinical studies conduct such as answers to IRBs and HA questions, protocol scientific and medical training, medical review of data within the scope of the Centralized
He/She will support the QA program to assure the accuracy and quality of scientific data submitted to regulatory agencies in support of new drug applications and/or biological licensing agreement applications. The R&D QA Manager will collaborate and
This is an exciting and challenging role where you will have technical ownership of commercially launched products and new product introductions to the site (spanning developmental studies and clinical manufacturing up to validation and
Provision of scientific and technical leadership to multidisciplinary teams to achieve corporate goals in challenging research projects within early-stage biologics drug development. Establishing and managing research projects as project scientist;
Responsible for understanding local treatment paradigms and standard of care to support targeted feasibility and strategic allocation of trials as required. Accountable for comprehensive site management activities to ensure timely delivery of enrolment