This role is primarily accountable for the end to end performance and project management for assigned protocols in a country in compliance with International Conference on Harmonization Good Clinical Practice (ICH/GCP) and country regulations, our company's policies and procedures, quality standards and adverse event reporting requirements internally and externally. Primary duties include, but are not limited to: Main Point of Contact for assigned protocols and links between Country Operations and clinical trial team. Accountable for project management of the assigned studies: pro-actively plans, drives, and tracks execution and performance of deliverables/timelines/results to meet country commitments from feasibility a
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