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Senior Local Trial Manager

TieTalent
Department:Project Management
Type:REMOTE
Region:UK
Location:Reading, England, United Kingdom
Experience:Mid-Senior level
Estimated Salary:£60,000 - £80,000
Skills:
CLINICAL TRIAL MANAGEMENTICH-GCPUK REGULATORY REQUIREMENTSSTUDY BUDGETSTIMELINESCROSS-FUNCTIONAL TEAMSVENDOR OVERSIGHTCHANGE CONTROL PROCESSES
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Job Description

Posted on: August 18, 2025

Location: UK, home-based Department: Clinical Operations As a Senior Local Trial Manager (LTM) at IQVIA, you’ll play a pivotal role in accelerating the delivery of innovative therapies to patients. You’ll lead the planning, execution, and oversight of regional clinical trials, ensuring quality, compliance, and operational excellence. This is your opportunity to work on cutting-edge medicines and shape the future of healthcare. Why Join IQVIA? 🏆 #1 in our category on the 2025 Fortune® World’s Most Admired Companies™ list — for the fourth year running! 🚀 Genuine career development opportunities in a global, growth-focused organization. 💊 Be part of transformational research that brings new treatments to market faster. Key Responsibilities Lead the delivery of regional clinical trials, ensuring timelines, quality, and budget targets are met. Develop and implement integrated study management plans in collaboration with cross-functional teams. Serve as the primary point of contact for sponsors, vendors, and internal stakeholders. Monitor project progress, proactively manage risks, and resolve issues to maintain study momentum. Drive financial performance by managing budgets, forecasting, and identifying revenue acceleration opportunities. Ensure compliance with ICH-GCP, local regulations, and company SOPs. Mentor and support junior team members, contributing to a culture of continuous learning and excellence. Represent IQVIA in bid defense meetings and client presentations for regional studies. What You’ll Bring Bachelor’s degree in Life Sciences or a related field. 3–5+ years of UK-based clinical trial management experience, including regulatory submissions. Strong knowledge of clinical trial conduct, ICH-GCP, and UK regulatory requirements. Proven ability to manage study budgets, timelines, and cross-functional teams. Excellent communication, leadership, and stakeholder management skills. Experience with vendor oversight and change control processes is a plus. Ready to make a difference? Apply today to join a team that’s passionate about improving lives through science. At IQVIA, your work has purpose — and your career has no limits. Please note: this role is not eligible for UK visa sponsorship. IQVIA is a leading global provider of clinical research services, commercial insights and healthcare intelligence to the life sciences and healthcare industries. We create intelligent connections to accelerate the development and commercialization of innovative medical treatments to help improve patient outcomes and population health worldwide. Learn more at https://jobs.iqvia.com

Originally posted on LinkedIn

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