
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.
🔥 1 minute ago
🏄 California, Connecticut – Remote
💵 $99k - $196k / year
⏰ Full Time
🟡 Mid-level
🟠 Senior
👔 Manager
🦅 H1B Visa Sponsor
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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.
• Lead, mentor, and develop a team of Clinical Database Programmers through performance management, training, and capability development • Coordinate project assignments, timelines, and resource allocation to ensure high-quality and timely delivery of database programming activities • Oversee EDC development and database configuration activities across internal and third-party platforms • Review database build specifications, edit check specifications, validation plans, and reconciliation requirements to ensure quality and compliance • Partner with sponsors, internal stakeholders, and external vendors to resolve issues, implement system enhancements, and support electronic data transfers • Guide database testing, validation, maintenance, and deployment activities in accordance with departmental procedures and standards • Contribute to the development of database libraries, system documentation, procedures, and best practices • Drive process improvements, provide technical leadership for new solutions, and support ongoing monitoring of study and system metrics • Support quality assurance, audit readiness, and continuous improvement initiatives across Clinical Database Programming
• Bachelor's degree or equivalent relevant education and experience • Experience leading or managing clinical database programming activities within a clinical research environment • Strong knowledge of EDC systems, database configuration, validation, testing processes, and data management workflows • Ability to review technical specifications, validation documentation, and database-related deliverables with a high level of accuracy • Strong problem-solving skills with a methodical and logical approach to identifying and resolving issues • Excellent attention to detail and a commitment to data quality and integrity • Strong communication, collaboration, stakeholder management, and customer-focused relationship-building skills • Proficiency in English and strong written and verbal communication skills
• Competitive benefits package depending on location • Transparent compensation and pay equity
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