Integral Study Manager – Clinical Operations
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 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.