Global Study Manager – Clinical Operations
Si le interesa solicitar este empleo, por favor, asegúrese de cumplir los siguientes requisitos que se enumeran a continuación.Remote |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: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 excellenceWhat We're Looking For:Proven experience managing global clinical trialsStrong vendor management expertise (CRO oversight essential)Ability xiphteb 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 CROWhat 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.