Associate Clinical Data Manager

🔥 8 minutes ago

🇬🇧 United Kingdom – Remote

⏰ Full Time

🟢 Junior

🟡 Mid-level

🧪 Clinical Research

🇬🇧 UK Skilled Worker Visa Sponsor

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

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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

• Support Lead Data Managers with study start-up, conduct, and close-out activities across assigned clinical trials • Prepare and maintain Data Management Plans, CRF Completion Guidelines, and Data Transfer Agreements • Perform and support user acceptance testing for new study database builds and mid-study updates • Review, clean, and validate clinical trial data for accuracy, completeness, and quality • Reconcile data from Serious Adverse Events, IRT systems, and central laboratories • Generate and maintain study reports according to study documentation and reporting requirements • Support database lock activities and timely study milestones and deliverables • Contribute feedback and recommendations to process improvement initiatives • Act as Lead Data Manager for one or more studies when required

🎯 Requirements

• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience • 1–3 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries • Proficiency in English • Strong attention to detail with a commitment to data accuracy and quality • Good written and verbal communication skills and ability to collaborate effectively with study teams • Basic knowledge of clinical data management methodologies, best practices, and technologies • Basic understanding of clinical trial processes and key study documents, including protocols, statistical analysis plans, CRFs, and study reports • Ability to manage assigned responsibilities effectively while contributing to the successful delivery of clinical trial data

🏖️ Benefits

• Collaborative and inclusive environment • Growth and career development opportunities • Opportunity to learn and expand technical expertise • Opportunity to take ownership of key study activities • Global work environment with collaboration across multiple time zones

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