As our Clinical Trials Manager, you will lead the execution and oversight of global clinical activities to support product development and post-market surveillance.
From planning through to closeout, you’ll ensure trials run smoothly, ethically, and efficiently – keeping patients at the centre of everything.
Managing internal teams, research partners, and investigational sites, you will deliver high-quality studies that meet global regulatory standards.
Beyond this, you will also shape the strategic direction of our research, translating cutting-edge science into meaningful, real-world outcomes.
Day to day, you’ll:
– Lead regulatory submissions and manage ethics approvals
– Oversee investigational product traceability and site documentation
– Identify and assess trial feasibility and lead site selection
– Review monitoring reports and address any issues that arise
– Manage site contracts, budgets, and investigator agreements
What We’re Looking For:
– At least 2 years’ experience in a commercial clinical trials role or at least 4 years’ experience as a Clinical Research Associate
– Proven experience managing global studies and overseeing clinical teams
– A strong understanding of GCP and international regulatory frameworks (MHRA, FDA, EU, ICH)
– Clear, confident communication skills and a collaborative mindset
– A PhD in Biological Sciences or a related field
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