Johnson & Johnson Careers: Apply Now for Analyst Position
Johnson & Johnson Careers: Johnson & Johnson is seeking an experienced Analyst II – Central Monitoring Manager to support its global clinical trial monitoring operations. The role is ideal for professionals with strong data analytics, central monitoring, and ARBM expertise who are passionate about improving clinical trial quality, participant safety, and operational efficiency across large-scale global studies.
Johnson & Johnson Careers: Job Details
- Position: Analyst II – Central Monitoring Manager
- Department: Data Analytics & Computational Sciences
- Sub-function: Clinical Data Management
- Category: Experienced Analyst (P5)
- Location: Mumbai / Hyderabad / Bangalore
- Work Pattern: Hybrid Work
About Johnson & Johnson
Johnson & Johnson is a global leader in healthcare innovation, delivering transformative solutions across pharmaceuticals and medical technology. With a mission to improve health for humanity, J&J drives pioneering research, develops advanced therapies, and manages end-to-end clinical operations across the world. Its India operations are a critical part of the global clinical development, data science, and risk-based monitoring ecosystem.
Johnson & Johnson Careers: Qualifications
- Bachelor’s degree required (Health Sciences)
- An advanced degree (master’s/PhD) is desirable.
- Experience in a pharmaceutical, biotech, or CRO environment.
- Strong understanding of RBQM/RBM, central monitoring, and ICH-GCP.
- Familiarity with statistical concepts, trial data analytics, and digital tools.
- Experience with data platforms used for collection, analysis, and reporting.
- Strong verbal and written communication skills in English.
- Ability to work cross-functionally and manage multiple communication streams.
Role Overview
The Analyst II – Central Monitoring Manager supports the execution of Analytical Risk-Based Monitoring (ARBM) activities for multiple clinical trials. This individual contributor role specializes in data analytics, risk detection, central monitoring processes, and trial quality oversight, working closely with global cross-functional teams.
Key Responsibilities
Core Central Monitoring Responsibilities
- Execute central monitoring activities across study start-up, execution, and close-out.
- Support ARBM processes and contribute to enhancements in monitoring models and methodologies.
- Ensure compliance with J&J SOPs, guidelines, and global regulatory requirements.
- Analyze trial data to identify risks, trends, deviations, and early warning signals.
- Collaborate with statisticians, programmers, data managers, and clinical teams to translate CtQ factors into meaningful reports.
- Escalate and communicate risks through defined governance pathways.
Role-Specific Responsibilities (Central Monitoring Manager)
- Support protocol risk assessment, protocol de-risking, and integrated risk management plans.
- Participate in cross-functional Central Monitoring Working Groups (CMWG).
- Review actions taken to investigate and resolve identified risks.
- Assist in developing and overseeing Study-Specific Reports (SSRs) and Central Statistical Surveillance (CSS) analytics.
