Clinical Trial Manager
Are you passionate about advancing clinical research?
As a Clinical Trial Manager, your expertise will shape the future of innovative treatments. This is an opportunity to work in a supportive, collaborative environment with opportunities for personal and professional growth. You will play a vital role in the development of industry-leading studies, contributing to cutting-edge research.
What You’ll Do
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Operational study management, ensuring time, cost, and quality deliverables are met with precision
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Independently manage all clinical research activities, overseeing studies from initiation to closeout
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Lead site selection, initiation, and activation, ensuring smooth site management
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Drive regulatory excellence by preparing and submitting HRA applications in the UK and supporting US approval processes
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Collaborate with data management teams and external vendors to deliver accurate, timely data
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Ensure clinical operations are inspection-ready, contributing to the development and review of study protocols, manuals, and regulatory documents
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Monitor quality through regular site communications and implement corrective action plans as needed
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Contribute to the development of the clinical quality management system
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Build strong relationships with investigators, CROs, and regulatory consultants, maintaining high standards of compliance and collaboration
What We’re Looking For
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A degree (or equivalent) in Biological Sciences, with a passion for clinical research
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3+ years of Clinical Trial Management experience in a commercial setting, or 4+ years as a Clinical Research Associate at a senior level
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Expertise in ICH/GCP guidelines and regulatory compliance in the EU and US
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Strong project management and problem-solving skills, with the ability to assess risks and propose creative solutions
Ready to make an impact? Apply now and become a part of our journey toward scientific discovery and innovation
