Johnson & Johnson is a global leader in healthcare innovation, spanning pharmaceuticals, medical devices, and consumer health. With a mission to profoundly impact health for humanity, J&J continues to build smarter, less invasive, and more personalized treatments.
💼 Job Role: Analyst II – Central Monitoring Expert
As part of the Clinical Data Management team within Data Analytics & Computational Sciences, you will contribute to Analytical Risk-Based Monitoring (ARBM) and central monitoring of clinical trials. Your efforts will ensure data quality and participant safety across global trials.
📌 Key Responsibilities
- Execute central monitoring for clinical trials from setup to close-out.
- Support ARBM model development and improvement initiatives.
- Ensure compliance with J&J SOPs and global regulations.
- Collaborate on development of study-specific reports, tools, and dashboards.
- Analyze Central Statistical Surveillance (CSS) data and identify risks.
- Help configure platforms and maintain central monitoring systems.
- Participate in cross-functional communication and innovation projects.
🎓 Eligibility Criteria
Education:
- Bachelor’s degree (BS/BA) in Health Sciences, Life Sciences, or Data Sciences.
- Master’s or PhD preferred.
Experience:
- Prior experience in Pharmaceuticals, Biotech, or CRO settings.
- Knowledge of RBQM/RBM, ICH-GCP, and clinical trial regulations.
- Familiarity with data analytics, statistics, and monitoring tools.
- Hands-on experience with clinical systems, dashboards, or reporting tools.
- Excellent verbal and written communication in English.
🎁 Job Benefits
- Competitive salary & incentives
- Hybrid work flexibility
- Global exposure and professional development
- Inclusive, innovation-driven work culture
- Employee health and wellness programs
- Access to industry-leading training and analytics platforms
📥 How to Apply
