Non-Clinical Job at Novo Nordisk
Are you ready to take on a challenging role in a leading healthcare organization? Novo Nordisk is offering an exciting non-clinical job opportunity as a Central Monitor in Bangalore. This Non-Clinical Job in Bangalore is ideal for those passionate about patient safety and regulatory compliance. With a focus on innovative therapies for chronic diseases, Novo Nordisk invites you to contribute to their mission of improving health outcomes globally.
About Novo Nordisk:
Novo Nordisk is a global healthcare company specializing in the development and production of innovative therapies for chronic diseases. With a strong commitment to patient care, the organization operates in the pharmaceutical sector, focusing on diabetes and other serious health conditions. Headquartered in Denmark, Novo Nordisk has a significant presence in Bangalore, India, where it fosters an environment of collaboration and innovation. This non-clinical job opportunity reflects the company’s dedication to improving health outcomes through rigorous research and development.
Job Details:
- Job Title: Central Monitor
- Department: Centralised Monitoring Unit
- Location: Bangalore, Karnataka, IN
- Category: Clinical Development
About the Non-Clinical Job:
As a Central Monitor, the successful candidate will play a crucial role in defining standard and trial-specific key risk indicators while performing ongoing monitoring of operational risks. This non-clinical job is pivotal in ensuring that both standard and trial-specific Key Risk Indicators (KRIs) impacting patient safety, data quality, and regulatory compliance are appropriately defined as per protocol and monitoring strategy prior to the start of centralized operational monitoring review.
Key Responsibilities:
- Perform ongoing centralized operational monitoring activities on assigned studies using vendor platform dashboards and outputs, in accordance with Novo Nordisk SOPs, ICH/GCP, and regulatory guidelines.
- Utilize advanced data visualization and analytics tools to proactively identify risks and drive data-driven decision-making in this Non-Clinical Job in Bangalore.
- Provide inputs to applications, databases, and systems used to monitor operational data.
- Communicate findings of operational review to relevant stakeholders to enable decision-making, acting as the primary contact for assigned centralized monitoring studies.
- Contribute to discussions and share learnings and best practices with wider CMU colleagues and other relevant stakeholders at Novo Nordisk Careers.
- Maintain knowledge of and act in compliance with global and local SOPs, GCP, and other regulatory requirements.
- Champion continuous improvement and innovation, sharing best practices and driving change across the department.
Your skills & qualifications:
The ideal candidate for this non-clinical job will possess analytical rigor, a quality mindset, and a passion for continuous improvement. To succeed in this role, candidates should bring:
- A minimum of a bachelor’s degree in life science, a scientific, or a healthcare discipline.
- 3+ years of relevant clinical research experience with a good knowledge of the drug development process and risk-based quality management (RBQM) principles.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines, particularly ICH-GCP E6 R2 and R3.
- Skill in aggregate data review and interpretation using visualization/analysis software.
- Strong communication and presentation skills, with the ability to interact proactively and professionally with colleagues and stakeholders.
- The ability to manage multiple projects and priorities independently under tight deadlines.
Prior CRA/field monitoring experience and hands-on experience with CluePoints solutions will be considered an advantage.
