Senior Clinical Data Manager

🔥 1 minute ago

🌲 North Carolina – Remote

🌲 North Carolina – Remote

💵 $79k - $157k / year

⏰ Full Time

🟠 Senior

🧪 Clinical Research

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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 end-to-end data management activities across multiple complex global projects and programs, from start-up through database lock and closeout • Develop Data Management Plans, database specifications, edit check specifications, CCGs, and Data Transfer Agreements • Oversee UAT, data cleaning, external vendor reconciliation specifications, and database lock activities • Allocate resources and monitor project scope, budgets, timelines, risks, and performance metrics, escalating concerns when appropriate • Represent Data Management in internal, sponsor, and study meetings • Collaborate with cross-functional teams and Data Management leadership to resolve challenges • Lead and contribute to process reviews and improvements • Train, support, and mentor Data Management team members • Participate in sponsor audits, regulatory authority inspections, and other third-party meetings as needed

🎯 Requirements

• Bachelor’s degree or higher in biomedical sciences, life sciences, computer science, or a related discipline, or equivalent relevant experience • Minimum of 5 years of experience in clinical data management or a related role within the pharmaceutical, biotechnology, or medical device industries • Strong knowledge of clinical data management best practices and technologies used in clinical trials • Strong understanding of clinical trial processes and key study documents, including protocols, statistical analysis plans, CRFs, and study reports • Proven ability to independently oversee projects, manage priorities, and solve complex problems with excellent attention to detail • Excellent communication and interpersonal skills, with the ability to collaborate effectively with internal and external cross-functional teams • Proficiency in English

🏖️ Benefits

• Competitive benefits package depending on location • Inclusive and equitable workplace • Equal employment opportunities • Opportunities to learn, grow, and shape the future of clinical research • Training, support, and mentorship opportunities

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