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!