Are you passionate about advancing healthcare through data analytics? Johnson & Johnson, a global leader in innovative medicine, is seeking a talented Analyst II Analytical Monitor to join its Integrated Data Analytics and Reporting (IDAR) team in Penjerla, Telangana. This hybrid role offers a unique opportunity to support clinical trials by leveraging cutting-edge data analytics, ensuring data reliability, and enhancing site performance. If you have a background in health sciences, data sciences, or clinical trial operations, this position is your chance to make a meaningful impact on global health. Apply by August 15, 2025, and be part of a team driving the future of healthcare innovation.
Key Responsibilities
As an Analyst II Analytical Monitor, you will play a pivotal role in ensuring the success of clinical trials through advanced data analytics and risk-based monitoring. Your responsibilities will include:
- Conducting analytical monitoring activities for multiple clinical trials, ensuring compliance with Johnson & Johnson’s Standard Operating Procedures (SOPs) and regulatory guidelines like ICH-GCP.
- Performing fit-for-purpose reviews at site and subject levels to detect issues early and prevent recurrence.
- Collaborating with Site Managers and Central Monitoring Managers to address trends and signals affecting data quality and study participant safety.
- Accessing various systems and databases to identify risks related to site and subject-level data quality and compliance.
- Providing timely analytical data insights to support Site Managers in prioritizing site engagement.
- Supporting process improvement projects, including requirements development, user acceptance testing, and identifying enhancements for analytical tools.
- Facilitating effective communication across cross-functional teams and managing escalation pathways as needed.
Qualifications
To excel in this role, candidates should meet the following requirements:
- Education: Bachelor’s degree (BS/BA) in Health Sciences, Data Sciences, or a related field. Advanced degrees (Masters, PhD) are preferred.
- Experience: Prior experience in the pharmaceutical, CRO, or biotech industry, with knowledge of clinical trial operations and study execution.
- Technical Skills: Familiarity with data analysis, basic statistical concepts, and technology platforms for data collection, analysis, and reporting.
- Regulatory Knowledge: Working knowledge of regulatory guidelines, such as ICH-GCP.
- Soft Skills: Strong critical thinking, problem-solving, and communication skills (written and verbal in English). Ability to collaborate effectively in a cross-functional environment.
- Preferred Skills:
- Experience with complex data structures, statistical analysis, data modeling, or data visualization.
- Knowledge of Risk-Based Quality Management (RBQM), Risk-Based Monitoring (RBM), or Quality by Design (QbD) concepts.
- Familiarity with external data (e.g., Safety Lab, PK, Simple Biomarkers, ECG).
Benefits of Working at Johnson & Johnson
Joining Johnson & Johnson offers a range of benefits designed to support your professional and personal growth:
- Innovative Environment: Work with cutting-edge technology and data analytics to drive healthcare breakthroughs.
- Hybrid Work Model: Enjoy the flexibility of a hybrid role, combining remote work with collaboration at our Penjerla facility.
- Career Growth: Access opportunities for professional development and involvement in process improvement projects.
- Global Impact: Contribute to clinical trials that shape the future of healthcare worldwide.
- Collaborative Culture: Work alongside experts in Innovative Medicine and MedTech, fostering meaningful partnerships.
How to Apply
