of designated deliverables and project timelines.Perform start up and site activation activities according to applicable regulations... sites.Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed...
of designated deliverables and project timelines.Perform start up and site activation activities according to applicable regulations... sites.Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed...
of designated deliverables and project timelines. Perform start up and site activation activities according to applicable... sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed...
of designated deliverables and project timelines. Perform start up and site activation activities according to applicable... sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed...
of designated deliverables and project timelines. Perform start up and site activation activities according to applicable... sites. Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed...
of designated deliverables and project timelines.Perform start up and site activation activities according to applicable regulations... sites.Review, track and follow up the progress, the approval and execution of documents, regulatory, ethics, Informed...
with empathy and we're committed to making a difference. Parexel FSP is looking for Global Site Start-up II in Argentina... Job Summary The Global Site Start-up II is accountable for the global execution of site activation for assigned clinical trials...
A leading healthcare clinical research organization in Buenos Aires seeks a Manager, Study Start-Up. In this role..., you will manage the end-to-end study start-up process, overseeing a team and ensuring compliance with regulations. Ideal candidates...
Study Start Up Associate II ICON plc is a world-leading healthcare intelligence and clinical research organization... initial start-up and maintenance submission packages to Central EC/IRB, Local EC/IRB, Competent Authorities, any other local...
Senior Study Start up Specialist, IQVIA Biotech page is loaded## Senior Study Start up Specialist, IQVIA Biotechtime... procedures (SOPs), Work Instructions (WIs), quality of designated deliverables and project timelines. • Perform start up and site...