Global Study Manager – Clinical OperationsRemote |Spain | Bulgaria | Greece | Hungary | Poland | Romania |We're partnering with a leading global biopharmaceutical organisation to find an experienced Global Study Manager (GSM) to support the delivery of complex, international clinical trials.This is a fantastic opportunity to play a key role within Clinical Operations, ensuring studies are delivered on time, within budget, and to the highest quality standards, from protocol development through to close-out and reporting.Key Responsibilities:
\n
Inscríbase ahora, lea los detalles del trabajo desplazándose hacia abajo. Verifique que posee las habilidades necesarias antes de enviar una solicitud.
\n
Lead end-to-end delivery of global clinical studiesCoordinate cross-functional teams and external partnersManage CROs and vendors to meet timelines, cost, and quality expectationsOversee study timelines, risks, and issue resolutionEnsure inspection readiness through high-quality TMF managementSupport study budgets and vendor invoice reconciliationCollaborate with Clinical Supply for timely study materialsContribute to study documentation and investigator meetingsDrive continuous improvement and operational excellence What We're Looking For:
\n
Proven experience managing general clinical trialsStrong vendor management expertise (CRO oversight essential)Ability xugodme to collaborate across global, cross-functional teamsExperience in risk management and escalation handlingSolid knowledge of ICH GCP and clinical trial regulationsBackground in Clinical Operations within a sponsor or CRO What to do next:If this opportunity is of interest, please apply now with your CV as the organisation are looking to welcome Clinical Project Manager s onboard as soon as possible.