About the CompanyI'm currently working with a CRO based in Spain for an exciting CTA role on a hybrid model.About the Role The idea is for the individual to transition from a CTA to a junior CPM.
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In this role, you would support clinical study teams with Trial Master File (TMF) management, document tracking, regulatory submissions, and general study coordination activities to ensure compliance and smooth trial execution.ResponsibilitiesSupport clinical study teams with Trial Master File (TMF) managementDocument trackingRegulatory submissionsGeneral xpzdshu study coordination activities to ensure compliance and smooth trial executionQualifications 4-5 years as a junior
- mid level CTARequired Skills Smartsheet management experience