Clinical Data Manager

🕒 October 7

🌐 United Kingdom, Spain, +4 more countries – Remote

🇬🇧 United Kingdom – Remote 🇪🇸 Spain – Remote 🇵🇱 Poland – Remote 🇷🇴 Romania – Remote 🇭🇷 Croatia – Remote 🇮🇹 Italy – Remote

⏰ Full Time

🟡 Mid-level

🟠 Senior

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

This company has sponsored UK Skilled Worker visas in the past.

👻 Ghost score 10%

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Worldwide Clinical Trials

WebsiteLinkedInAll Job Openings

1001 - 5000 employees

🏥 Healthcare

💼 Consulting

📦 Logistics

Healthcare • Consulting • Logistics

Worldwide Clinical Trials is a global contract research organization (CRO) that provides comprehensive clinical trial services. They specialize in supporting studies across diverse therapeutic areas such as oncology, cardiology, and rare diseases. With over 30 years of experience, Worldwide Clinical Trials emphasizes personalized support and customized solutions throughout the entire lifecycle of drug development. Their services include clinical monitoring, data management, patient recruitment, and regulatory consulting, ensuring precision and tailored attention for each clinical trial.

📋 Description

• 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

🎯 Requirements

• 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 commitment to data quality • Strong analytical and problem-solving skills • Excellent written, verbal, interpersonal, and cross-functional collaboration skills across global teams