NonStop Consulting
Clinical Project Manager
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About the Role
Our client, a global Contract Research Organisation, is entering an exciting growth phase in Europe following a recent strategic acquisition. With an established presence across Asia-Pacific and North America, they are now expanding their European footprint and investing in an experienced Clinical Project Manager to lead this next chapter. You'll join a people-focused, award-winning employer that backs your development with structured mentorship, leadership pathways, and exposure to complex, international oncology clinical trials.
Benefits
- Remote-first flexibility with real autonomy: work fully remotely within the UK, supported by a flexible benefits framework designed to help you build a sustainable work-life balance.
- Lead end-to-end delivery of international clinical trials, with a particular focus on supporting and growing the European region while improving patient outcomes worldwide.
- Work on interesting and challenging early phase clinical trials
Role Responsibilities
- Lead global and European clinical projects end-to-end: own planning, execution, and delivery of international clinical trials, helping to strengthen and scale the organisation's European operations while meeting quality, timeline, and budget goals.
- Be the primary sponsor interface: act as the key client contact, driving governance meetings, managing expectations, overseeing budgets and risk management, and building strong, long-term sponsor partnerships in Europe and beyond.
- Drive team leadership and process excellence: lead and mentor global clinical project teams, including Associate Project Managers, while contributing to SOP and process improvements that support efficient, high-quality growth across the expanding European portfolio.
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Requirements
- Multiple years of clinical Project Management experience (from start-up to close-out)
- Significant experience managing global or regional clinical trials within a CRO, pharmaceutical, or biotechnology company
- Strong experience with oncology studies or similar complex studies
- Experience managing project budgets, timelines, resources, forecasting, risk management, and change orders.
- Comprehensive understanding of the clinical trial lifecycle, including site start-up, monitoring, recruitment, study close-out, and audit readiness.
- Strong knowledge of ICH-GCP, global regulatory requirements, and clinical trial management systems (e.g. CTMS, eTMF).
- Fluent level of English
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If this job appeals to you please apply here or send your CV to me, Annelies De Baere, on the NonStop Consulting website or on my Linkedin. If you are not available but you know someone that would be interested, please forward this to them and help the people in your network.
Do you have any disability or condition that could affect you in the application and interview process? Please feel free to share this information as part of your application, including any necessary adjustments you might need, so we can help make the process easier for you. We assure you this information will not have any negative effect on the interview process outcome.
About NonStop
We are NonStop, a leading provider of staffing solutions throughout Europe and now also in the US. We're passionate about connecting talent with opportunity and work non-stop to support our clients in hiring the best talent for their teams. Feel free to pop over to our website, NonStop Consulting, for more information, to browse all our roles, or to let us know how we can help you.
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