Clinical Data Manager (UK/Europe)

Worldwide Clinical Trials6 LocationsonsiteSalary not postedView the original posting at Worldwide Clinical Trials ↗

Who we are We’re a global, midsize CRO that pushes boundaries, innovates and invents because the path to a cure for the world’s most persistent diseases is not paved by those who play it safe. It is built by those who take pioneering, creative approaches and implement them with quality and excellence. We are Worldwide Clinical Trials, and we are a global team of over 3,500+ experts, bright thinkers, dreamers and doers and, together, we are changing the way the world experiences CROs – in the best possible way. Our mission is to work with passion and purpose every day to improve lives and we are looking for others who value this same pursuit. Why Worldwide We believe everyone plays an important role in making a world of difference for patients and their caregivers. From our hands-on, accessible leaders, to our cohesive and supportive teams, we are committed to enabling professionals from all backgrounds and experiences to succeed. We prioritize cultivating a diverse and inclusive environment that continues to promote collaboration and creativity. We are proud to be a workplace where people thrive by being themselves and are inspired to do their best work every day. Join us! Make an Impact as a Clinical Data Manager at Worldwide Play a key role in delivering high-quality clinical trial data that supports important research and development programmes around the world. In this position, you will provide data management expertise across complex global studies, helping ensure projects are delivered accurately, efficiently, and in line with sponsor expectations. Working closely with cross-functional teams, vendors, and stakeholders, you will oversee critical data management activities from study start-up through database lock. Your expertise will help drive data quality, support study progress, and contribute to the successful delivery of clinical research programs. As a trusted partner within global project teams, you will have the opportunity to influence processes, support continuous improvement, and help ensure data integrity throughout the clinical trial lifecycle. Where You'll Work This is a remote role open to candidates based in UK, Spain, Poland, Romania, Croatia or Italy. You will collaborate with global teams across multiple time zones. What You'll Do Lead data management activities across multiple complex global clinical trials from start-up through study close-out Coordinate resources and priorities to ensure data management deliverables are completed on time and within budget Develop and maintain key trial documentation, including data management plans, database specifications, edit check specifications, CCGs, and DTAs Oversee user acceptance testing (UAT) activities to support accurate and reliable database functionality Manage external vendor reconciliation specifications and support reconciliation outputs across study data sources Drive data cleaning activities to maintain data quality, consistency, and readiness for analysis Produce and communicate study metrics to monitor progress, identify risks, and support informed decision-making Partner with sponsors, vendors, and internal stakeholders while representing Data Management at project and study meetings Support continuous improvement initiatives by contributing feedback, participating in process reviews, and helping optimise data management practices What You'll Bring Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience Minimum 3 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries Proficiency in English Strong working knowledge of clinical data management best practices and technologies used in clinical trials Solid understanding of clinical trial processes and key study documents, including protocols, CRFs, statistical analysis plans, and study reports Excellent attention to detail and comm

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