Associate Director, Clinical Data Management

Job not on LinkedIn

🔥 0 minutes ago

🌐 United Kingdom, Bulgaria, +3 more countries – Remote

🇬🇧 United Kingdom – Remote 🇧🇬 Bulgaria – Remote 🇵🇱 Poland – Remote 🇭🇷 Croatia – Remote 🇷🇴 Romania – Remote

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

🇬🇧 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

• Oversee management teams to ensure compliance with SOPs on assigned projects and provide team, project, and budget oversight • Support development and implementation of department initiatives • Provide leadership, managerial, and technical expertise to the Data Management department • Ensure efficient, accurate, and timely completion of Data Management deliverables • Ensure departmental operations comply with applicable regulations, GCP, Worldwide SOPs and guidelines, and sponsor requirements • Provide line management for assigned management teams • Define and monitor objectives for assigned Managers and ensure career and personal development opportunities • Contribute to strategic department management • Oversee resourcing for assigned teams through proactive and strategic resource assignment • Oversee departmental quality and issue management by identifying trends and initiating strategic solutions • Manage departmental project deliverables, review project status, and establish mitigation plans • Monitor and manage project profitability and overburn/underburn for department projects • Oversee Subject Matter Experts for effective process oversight • Represent the department to internal and external stakeholders on strategic planning, oversight, risks, and mitigations • Develop and implement departmental SOPs • Lead development of departmental process improvement and efficiency initiatives • Perform other duties as assigned

🎯 Requirements

• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science or related discipline — or equivalent relevant experience • Minimum of 12 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries • 6–8 years of line management experience • Expert knowledge of data management best practices and technologies as applied to clinical trials • Advanced understanding of clinical trial processes and protocol documents, including protocols, statistical analysis plans, CRFs, and study reports • Strong project management skills and experience managing data management teams and projects for operational and budget oversight • Significant line management experience, including recruitment, career development, and performance reviews • Excellent attention to detail • Excellent written and verbal communication skills • Excellent communication and interpersonal skills for collaboration with cross-functional internal and external teams • Expert independent analytical and problem-solving skills