Worldwide Clinical Trials
Biotechnology • Pharmaceuticals • Healthcare Insurance
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.
Clinical Database Designer
October 31
🇬🇧 United Kingdom – Remote
⏰ Full Time
🟡 Mid-level
🟠 Senior
✍️ Designer
🇬🇧 UK Skilled Worker Visa Sponsor
Worldwide Clinical Trials
Biotechnology • Pharmaceuticals • Healthcare Insurance
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
• Provide support in planning, directing, and managing the clinical database design and maintenance process. • Work closely with the Lead Data Manager in the development of the clinical database design timeline. • Review the protocol and associated study reference materials for assigned studies to determine the specific database design requirements. • Design and review electronic case report forms (eCRFs) and support the set up of electronic data capture (EDC) systems for assigned projects in adherence with protocol requirements. • Author and review the Edit Check Specifications for assigned projects. • Work closely with the Lead Data Manager and Clinical Database Programmer to ensure accurate implementation of database design and edit check requirements. • Lead sponsor meetings to review draft eCRFs and ensure all sponsor requirements are addressed.
🎯 Requirements
• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience. • Three to five years' experience in protocol interpretation and designing clinical databases, including Medidata Rave and/or Merative Zelta. • Familiarity with CDISC and CDASH standards.
🏖️ Benefits
• Collaborative environment • Diverse and inclusive workspace • Professional growth and development opportunities
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