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 studies
* Coordinate cross-functional teams and external partners
* Manage CROs and vendors to meet timelines, cost, and quality expectations
* Oversee study timelines, risks, and issue resolution
* Ensure inspection readiness through high-quality TMF management
* Support study budgets and vendor invoice reconciliation
* Collaborate with Clinical Supply for timely study materials
* Contribute to study documentation and investigator meetings
* Drive continuous improvement and operational excellence
What We’re Looking For:
* Proven experience managing global clinical trials
* Strong vendor management expertise (CRO oversight essential)
* Ability xhfqzwm to collaborate across global, cross-functional teams
* Experience in risk management and escalation handling
* Solid knowledge of ICH GCP and clinical trial regulations
* Background 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.