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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

The Clinical Trial Assistant will perform daily administrative activities, in conjunction with the Clinical Research Associates and Regulatory and Start-Up teams, to ensure a complete and accurate Trial Master File delivery. IQVIA are seeking a Clinical Trial Assistant to join us on our mission to d

They are responsible for formal clinical trial monitoring to ensure trials are conducted, recorded and reported in adherence with the Protocol, SOPs and relevant Regulatory Guidance such as Good Clinical Practice. Ensure clinical trials are conducted, recorded and reported in adherence with the Prot

Applies knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager. May assist in the review of study-related documents as they relate to the supported clinical trials as delegated by the Regional Clinical Study Manager (e. Acquires regional study man

The aCTM will be part of the Clinical Trial Management team working with Project Coordinators and Clinical Trial Managers in performance of clinical trial management activities. Medpace is currently seeking candidates with PhDs and/or Post-Doctoral Research experience for a full-time, office-based A

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Minimum of 7 years in clinical research in a CRO or Pharmaceutical/Biotechnology I

Applies knowledge of clinical trials operations in the region under guidance of the Regional Clinical Study Manager. May assist in addressing routine study questions from clinical trial sites. Oversees multiple aspects of clinical trial conduct at the regional level, including feasibility, study sta

As a Clinical Trial Manager, you will be joining the world’s largest & most comprehensive clinical research organisation, powered by healthcare intelligence. Lead and manage the conduct of clinical trials from start-up to closeout in accordance with ICH-GCP and local regulations. Collaborate with

Reporting to our VP of Sales & Marketing in Paris, you will be responsible for selling our Pharmacovigilance and Clinical Trials solutions to clients in the life sciences and healthcare sectors located in Europe, and potentially in Asia. Sales Executive – Pharmacovigilance/Clinical Trial IT Soluti

Join to apply for the Clinical Trial Manager - Oncology - EU - Remote role at Worldwide Clinical Trials. Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role. Clinical Trial Manager - Oncology - EU - Remote.

Drives and leads the successful execution, oversight and approval of all clinical trial documents and operational plans of global clinical trials using strong project management, leadership, and organizational skills. Minimum of 7 years in clinical research in a CRO or Pharmaceutical/Biotechnology I

Support the Global Clinical Trial Manager, Global Early Clinical Development Manager, Local Trial Manager, Regional or Country Study Manager in the delivery of the clinical and operational strategy and assist the execution of clinical trials. Work with the clinical trial management staff to support

Ensures accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical tria

Ensure accurate and up-to-date trial information within relevant tracking systems and provide regular updates of trial progression to Clinical Operations Lead, Clinical Trial Lead, and other defined stakeholders. Must have knowledge of protocol and clinical drug development processes, clinical trial

With clinical trials conducted in 100+ countries and ongoing development of novel frameworks for clinical research through our PPD clinical research portfolio, our work spans laboratory, digital and decentralized clinical trial services. Our global Clinical Operations colleagues within our PPD clini

Clinical Trial Managers (CTMs) and Clinical Research Associates (CRAs) play a vital role in ensuring our clinical research programs are executed with the quality and excellence our sponsors expect and the care and passion patients deserve. Clinical Trial Manager, Clinical Operations Leader, Lead CRA

With over 25 years of experience in vaccine research, the Oxford Vaccine Group undertakes vaccine research at all stages of the process from pre-clinical development to late phase policy influencing trials, with the sole aim of ensuring protection of as many individuals as possible from vaccine prev

Join Worldwide Clinical Trials for an unparalleled CRO experience, where you can drive extraordinary scientific breakthroughs and contribute to the very heart of every successful clinical trial. Clinical Trial Manager, Clinical Operations Leader, Lead CRA, or equivalent role. We are Worldwide Clinic