Clinical Trial Manager, (Oncology Experience Required) - UK at Parexel

About this role

When our values align, there's no limit to what we can achieve. At Parexel , we all share the same goal - to improve the world's health. From clinical trials to regulatory, consulting, and market access, every clinical development solution we provide is underpinned by something special - a deep conviction in what we do. Each of us, no matter what we do at Parexel , contributes to the development of a therapy that ultimately will benefit a patient. We take our work personally, we do it with empathy and we're committed to making a difference. About Parexel
Parexel is a leading global clinical development partner delivering insights driven clinical and consulting solutions to the life sciences industry. With 22,000+ employees worldwide, we partner with companies and research sites to design and deliver patient focused clinical trials that broaden access and make research a care option for anyone, anywhere. We work with focus, agility, and shared purpose, moving with urgency to address patient needs and accelerate the delivery of new therapies. We embrace bold thinking, adapt quickly to change, and continually raise the bar for the speed and quality of clinical research. We are expanding our team and seeking talented individuals to help drive industry leading innovation, With Heart®. About the Role We are seeking a local Clinical Trial Manager with oncology experience, to join our team in the UK in a remote capacity. This role is dedicated to a single client and offers the opportunity to play a critical leadership role in delivering country level clinical trials that help advance innovative treatments for patients. As a local Clinical Trial Manager, you will lead local study delivery, oversee operational execution, and ensure studies are conducted in compliance with applicable regulations, quality standards, timelines, and budgets. Working closely with cross functional teams, you will drive study performance, support regulatory and ethics submissions, and contribute directly to the successful delivery of clinical research programs. You will join a fast paced, growth-oriented environment supporting impactful clinical studies for leading biotechnology and pharmaceutical organizations. Whether your long-term interests lie in clinical operations, project management, line management, or broader leadership opportunities, this role provides a strong platform for continued professional development and career growth. Key
Deliver committed country level components of clinical studies within agreed timelines, budgets, and resource plans while ensuring compliance with client procedures, ICH-GCP guidelines, and local regulations.
Lead and optimize the performance of Local Study Teams at country level to support successful study execution and quality outcomes.
Manage country level study budgets and maintain accurate financial information through regular review of study financial systems and reports.
Ensure timely preparation of country financial Study Management Agreements (fSMA).
Oversee the preparation of country level Master Informed Consent Forms (MICF), site specific informed consent documentation, and associated translations as required.
Ensure timely submission of applications and study related documentation to Ethics Committees (EC) and Institutional Review Boards (IRB) throughout the study lifecycle.
Collaborate with internal and external stakeholders to ensure efficient study delivery and effective cross functional partnership.
Support study quality and operational excellence while maintaining compliance with regulatory requirements and client standards.
Candidate Profile You will thrive in this role if you bring:
Strong leadership, team motivation, and stakeholder management capabilities
Experience working within clinical research and local clinical trial delivery environments
The ability to collaborate effectively across cross functional teams
Excellent organizational, time management, and problem-solving skills, with the ability to manage multiple priorities
A quality focused approach and commitment to regulatory compliance and study excellence
Confidence working with study financial systems, regulatory processes, and clinical trial documentation
Required Qualifications
Bachelor's degree or equivalent experience in a relevant scientific, healthcare, or clinical research discipline
Minimum of 3 years' experience running local clinical trials
Experience in oncology clinical trials
Proven ability to lead and motivate cross functional teams to deliver clinical trials on time, within budget, and to required quality standards
Good understanding and working knowledge of clinical research, clinical trial phases, ICH-GCP, and applicable country clinical research regulations and guidelines
Experience performing submissions to Regulatory Authorities (RA) and Ethics Committees (EC)
Strong communication, organization, and problem-solving skills
Preferred Qualifications
Monitoring experience within oncology clinical studies
Experience partnering with study functions to support smooth and effective study delivery
Benefits and Compensation
Medical & Dental Insurance
Life Assurance
Pension
Critical Illness Insurance & Health Screenings
We offer a comprehensive benefits package to eligible employees, which includes life assurance, medical and dental insurance, and additional benefit offerings in accordance with the terms of our applicable plans. If this job does not sound like the next step in your career, but perhaps you know someone who would be a perfect fit, send them the link to apply. We believe in flexibility, growth, and creating space for people to do their best work. Join us and be part of a team where your contributions help shape the future of clinical research. Originally posted on Himalayas