Global Study Manager – Clinical Operations
Remote
FSP - Leading Global pharma
We’re supporting a leading global biopharmaceutical organisation in the search for an experienced Global Study Manager (GSM) to support the delivery of complex, global clinical trials.
This role sits within Clinical Operations and plays a key part in ensuring studies are delivered on time, within budget, and to the highest quality standards, from protocol development through to study close-out and reporting.
Key Responsibilities
* Support end-to-end delivery of global clinical studies from set-up through to close-out and CSR
* Coordinate cross-functional teams and external partners to ensure efficient study execution
* Manage global vendors (including CROs) to ensure performance against timelines, cost, and quality
* Contribute to study documentation (e.G. ICFs, study agreements, vendor specifications)
* Oversee study timelines, risks, and issue resolution, implementing mitigation plans where needed
* Ensure inspection readiness through high-quality Trial Master File (TMF) management
* Support study budget tracking, including vendor invoice reconciliation
* Collaborate with Clinical Supply to ensure timely provision of investigational product and study materials
* Contribute to investigator and study team meetings
* Drive continuous improvement initiatives and operational excellence activities
Key Requirements
* Experience managing global clinical studies across multiple regions
* Strong vendor management experience, including oversight of CROs and external providers
* Proven ability to work cross-functionally with global stakeholders
* Experience in risk management and escalation handling
* Solid understanding of ICH GCP and clinical trial regulations
* Background in Clinical Operations within a sponsor or CRO environment
What to do next:
If this opportunity is of interest, please apply direct or share a copy of your CV to
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