Pracovné ponuky vychádzajú z reálnych inzerátov, ich štruktúru a požiadavky však zjednocujeme pomocou umelej inteligencie (AI). Občas tak môže vzniknúť drobná nepresnosť spôsobená AI alebo nejasným zadaním v pôvodnom inzeráte. Pri odpovedi sa, prosím, držte celkového zmyslu ponuky a reagujte čo najkonkrétnejšie.

Odporučte konkrétneho kandidáta alebo zdieľajte tento inzerát. Vyberte si spôsob a odmena je Vaša.

Odporučte konkrétneho kandidáta alebo zdieľajte tento inzerát. Vyberte si spôsob a odmena je Vaša.
Information about the position Job description, responsibilities and duties Key ResponsibilitiesSite & Study OperationsConduct or support site selection, initiation, monitoring, and close-out visitsEnsure compliance with protocols, ICH-GCP, and regulatory standardsMonitor patient recruitment, data collection, and site performanceMaintain accurate trial documentation and audit readinessLiaise with the internal team for study coordination and reportingSite & Investigator ManagementBuild and maintain strong working relationships with investigators and site staffProvide protocol and GCP training to site teams when requiredSupport ethics submissions and site-level regulatory processesDocumentation & ComplianceTrack site status and ensure timely resolution of queriesEnsure all documentation is inspection-ready and compliant with internal SOPsParticipate in project meetings and provide site-level updates Employee perks, benefits Benefits:Flexible working hoursSick Days/Paid Time OffLaptop for Office useFree Drinks( coffee, Tea, Water)Health Insurance Employee TrainingAny additional benefits specified by the law.