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 Operational study management, ensuring time, cost, and quality deliverables are met with precision Independently manage all clinical research activities, overseeing studies from initiation to closeout Lead site selection, initiation, and activation, ensuring smooth site management Drive regulatory excellence by preparing and submitting HRA applications in the UK and supporting US approval processes Collaborate with data management teams and external vendors to deliver accurate, timely data Ensure clinical operations are inspection-ready, contributing to the development and review of study protocols, manuals, and regulatory documents Monitor quality through regular site communications and implement corrective action plans as needed Contribute to the development of the clinical quality management system Build strong relationships with investigators, CROs, and regulatory consultants, maintaining high standards of compliance and collaboration What We’re Looking For A degree (or equivalent) in Biological Sciences, with a passion for clinical research 3 years of Clinical Trial Management experience in a commercial setting, or 4 years as a Clinical Research Associate at a senior level Expertise in ICH/GCP guidelines and regulatory compliance in the EU and US 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