Who We AreWe’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.Who We AreWe’re a general, 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 WorldwideWe 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 WorldwidePlay 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 programmes. 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 WorkThis 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 DoLead data management activities across multiple complex global clinical trials from start-up through study close-outCoordinate resources and priorities to ensure data management deliverables are completed on time and within budgetDevelop and maintain key trial documentation, including data management plans, database specifications, edit check specifications, CCGs, and DTAsOversee user acceptance testing (UAT) activities to support accurate and reliable database functionalityManage external vendor reconciliation specifications and support reconciliation outputs across study data sourcesDrive data cleaning activities to maintain data quality, consistency, and readiness for analysisProduce and communicate study metrics to monitor progress, identify risks, and support informed decision-makingPartner with sponsors, vendors, and internal stakeholders while representing Data Management at project and study meetingsSupport continuous improvement initiatives by contributing feedback, participating in process reviews,



and helping optimise data management practicesWhat You'll BringBachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experienceMinimum 3 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industriesProficiency in EnglishStrong working knowledge of clinical data management best practices and technologies used in clinical trialsSolid understanding of clinical trial processes and key study documents, including protocols, CRFs, statistical analysis plans, and study reportsExcellent attention to detail and commitment to data qualityStrong analytical and problem-solving skillsExcellent written, verbal, interpersonal, and cross-functional collaboration skills across global teamsWe love knowing that someone is going to have a better life because of the work we do.To view our other roles, check out our careers page at Discover a world of difference at Worldwide! For more information on Worldwide, visit www.Worldwide.Com or connect with us on LinkedIn.Worldwide is an equal opportunity employer that is committed to enabling professionals from all backgrounds and experiences to succeed and, to that end, we prioritize attracting diverse talent and cultivating an inclusive environment that encourages collaboration and creativity. We know that when our employees feel appreciated and included, they can be more creative, innovative, and successful. We’re on a mission to hire the very best and are committed to creating exceptional employee experiences where everyone is respected and has access to equal opportunity. We provide equal employment opportunities to all employees and applicants regardless of race, color, ethnicity, ancestry, religion, national origin, gender, sex, gender identity or expression, sexual orientation, age, citizenship, marital or parental status, disability, military status, or other class protected by applicable law.#J-18808-Ljbffr

📌 Clinical Data Manager (Uk/Europe) (Madrid)
🏢 Worldwide Clinical Trials
📍 Madrid