Global Study Manager – Clinical Operations
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Remote |Spain | Bulgaria | Greece | Hungary | Poland | Romania |
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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.
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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.
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Key Responsibilities:
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- Lead end-to-end delivery of general 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
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What We’re Looking For:
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- Proven experience managing global clinical trials
- Strong vendor management expertise (CRO oversight essential)
- Ability xugodme 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
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What to do next:
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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.