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