Associate Director, Clinical Data Management

🔥 2 minutes ago

🦌 Connecticut, New York, +3 more states – Remote

🦌 Connecticut – Remote 🗽 New York – Remote 🌲 North Carolina – Remote 🍂 Massachusetts – Remote ⚓ Rhode Island – Remote

💵 $118.5k - $235.5k / year

⏰ Full Time

🟠 Senior

👨‍⚕️ Medical Director

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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 and mentor Data Management leaders, fostering team performance, engagement, and professional development • Drive compliance with applicable regulations, GCP, sponsor requirements, and Worldwide SOPs • Oversee resource allocation and workforce planning • Monitor project delivery, identify risks, and implement mitigation strategies • Manage departmental quality and issue management processes • Provide strategic oversight of project budgets, profitability, and resource utilization • Partner with internal and external stakeholders on project planning, risk management, and operational decision-making • Lead development, implementation, and continuous improvement of departmental processes, SOPs, and efficiency initiatives • Guide Subject Matter Experts and management teams in consistent execution of Data Management best practices

🎯 Requirements

• Bachelor's degree or higher in biomedical sciences, life sciences, computer science, or a 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 responsibility • Experience developing high-performing teams • Expert knowledge of clinical data management practices, technologies, and regulatory expectations applicable to clinical trials • Advanced understanding of clinical trial processes and key study documents, including protocols, CRFs, statistical analysis plans, and study reports • Strong project and budget management experience with demonstrated oversight of multiple projects and resources • Excellent analytical, problem-solving, communication, and interpersonal skills • Proficiency in English

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Professional development and growth opportunities • Collaborative work environment • Equal employment opportunities

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