Medical Monitor Job at Novo Nordisk
A rare chance has emerged for healthcare professionals as Novo Nordisk seeks a Central Monitor in Bangalore. This role offers an opportunity to engage in clinical development, with a focus on operational risk monitoring and patient safety. As Central Monitor, the selected candidate will be responsible for providing inputs in defining standard and trial-specific key risk indicators and performing ongoing monitoring of operational risks. This Medical Monitor Job involves ensuring that both standard and trial-specific Key Risk Indicators (KRIs) that impact patient safety, data quality, and regulatory compliance are appropriately defined in accordance with the protocol and monitoring strategy prior to the start of centralised operational monitoring review.
About Novo Nordisk:
Novo Nordisk is a global healthcare company headquartered in Denmark, renowned for its commitment to defeating serious chronic diseases such as diabetes. With a strong focus on research and development, the organisation integrates innovative scientific ideas with advanced technologies to deliver transformative therapies. The company operates in various countries, including India, where it emphasises collaboration and operational excellence in clinical trials.
Job Details:
- Department: Centralised Monitoring Unit
- Location: Bangalore, Karnataka, IN
- Category: Clinical Development
- Deadline: 26 October 2026.
Key Responsibilities:
- Performing ongoing centralized operational monitoring activities on assigned studies using vendor platform dashboards and outputs, in accordance with Novo SOPs, ICH/GCP, and regulatory guidelines and directives as part of this Medical Monitor Job.
- Utilising advanced data visualisation and analytics tools to proactively identify risks and drive data-driven decision-making.
- Providing inputs to applications, databases, and systems used to monitor operational data.
- Communicating findings of operational review to relevant stakeholders to enable decision-making, acting as the primary contact and participating in project meetings for assigned centralised monitoring studies.
- Contributing to discussions and sharing learnings and best practices with wider CMU colleagues and other relevant stakeholders.
- Maintaining knowledge of and acting in compliance with global and local SOPs, GCP, and other regulatory requirements.
- Championing continuous improvement and innovation, sharing best practices, and driving change across the department.
Skills & Qualifications Required for the Medical Monitor Job:
To succeed in this role, candidates should possess:
- A minimum of a bachelor’s degree in a healthcare discipline or a related field.
- 3+ years of relevant clinical research experience with a good knowledge of the drug development process and risk-based quality management (RBQM) principles, including demonstrated experience applying RBQM principles in clinical trial operations.
- In-depth knowledge of Good Clinical Practice (GCP) guidelines, with particular focus on ICH-GCP E6 R2 and R3, and a solid understanding of clinical trial design, execution, and operations.
- Skill in aggregate data review and interpretation using visualization/analysis software, along with a basic understanding of AI tools and their application in clinical operations.
- Strong communication and presentation skills, with the ability to interact proactively and professionally with colleagues, stakeholders, and management across cross-functional, culturally diverse teams.
- The ability to manage multiple projects and priorities independently under tight deadlines, with strong attention to detail, proactivity, and resilience to change.
Prior CRA/field monitoring experience and hands-on experience with CluePoints solutions will be considered an advantage. This Medical Monitor Job suits candidates with strong centralised monitoring, RBQM, and clinical trial operations experience.
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