• Lead end-to-end clinical data management activities for global clinical trials
• Collaborate with external vendors, internal teams, and trial stakeholders to align data management expectations
• Gather, review, and finalize requirements for eCRFs and clinical data collection tools
• Establish data quality standards, conventions, and ensure regulatory compliance
• Set, track, and manage data management timelines and milestones
• Ensure real-time inspection readiness and timely data deliverables
• Review clinical data management documents, reports, and submission packages
• Perform complex data reviews and manage queries in EDC systems
• Work closely with Study Responsible Scientists (SRS), physicians, and clinical working groups
• Contribute to process, system, and tool improvement initiatives
• Bachelor’s degree (BS/BA) in Clinical Data Management, Health Sciences, Computer Sciences, or related field
• Master’s degree or PhD preferred
• Around 2 years of experience in pharmaceutical, CRO, or biotech industry
• Experience in clinical drug development and clinical data management
• Strong written and verbal communication skills (English)
• Good understanding of clinical trial protocols and data management processes
• Ability to work effectively with cross-functional and global teams
• Knowledge of international clinical data management guidelines
• Familiarity with data capture platforms, EDC systems, and data privacy regulations
• Team leadership exposure preferred
• Willingness to travel up to 10% (domestic/international)
Johnson & Johnson is a global healthcare leader committed to transforming lives through innovative medicines, medical devices, and data-driven healthcare solutions. With a strong focus on clinical research and patient outcomes, the company plays a critical role in advancing global health through science, technology, and collaboration.
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