Job Opening for Dose Surveillance Advisor at Novo Nordisk in Bangalore
A rare chance has emerged for qualified candidates seeking a Novo Nordisk job opportunity in Bangalore as a Dose Surveillance Advisor in Bangalore, Karnataka. This role, part of the Centralised Monitoring Unit within Research & Development, focuses on dose surveillance across global clinical trials. The application deadline is 20 October 2026.
About the Company
Novo Nordisk is a global healthcare company with a focus on diabetes care, obesity care, and hormone replacement therapy. It operates in the pharmaceutical sector, developing and manufacturing innovative medications and solutions for patients worldwide. The company is headquartered in Denmark and has a significant presence in India, contributing to research and development in the life sciences field.
Job Details
- Company: Novo Nordisk
- Position: Dose Surveillance Advisor
- Department: Centralised Monitoring Unit, Research & Development
- Category: Clinical Development
- Location: Bangalore, Karnataka, India
- Experience: 1–2 years
- Qualification: Postgraduate degree in Life Sciences
- Deadline: 20 October 2026
Job Description: Novo Nordisk Bangalore Role
The Dose Surveillance Advisor will maintain a data-driven view of dose compliance across assigned clinical trial sites and support timely resolution and documentation of dose-related issues. This Novo Nordisk job Bangalore role involves overseeing compliance with prescribed dose status, conducting routine and ad-hoc dose surveillance reviews, and collaborating with trial teams to ensure adherence to protocols.
Key Responsibilities
- Oversee compliance with prescribed dose status across assigned trial sites.
- Conduct routine and ad-hoc dose surveillance reviews according to protocol requirements.
- Identify differences between prescribed and expected doses.
- Follow up with stakeholders and support sites through communication, data insights, and timely escalation.
- Work with Trial Managers on dose- and retention-related matters.
- Share findings with trial squads and medical partners.
- Document dose-related operational risks in relevant tools.
- Maintain inspection-ready records.
- Contribute to continuous improvement of the dose surveillance function.
Eligibility for Dose Surveillance Advisor Role
- Postgraduate degree in Life Sciences; M.Pharm, PharmD, MDS, or MSc Nursing preferred.
- 1–2 years of experience working with patient data in a hospital, clinical trial site, pharma, biotech, or CRO setting.
- Strong knowledge of clinical trial conduct and ICH-GCP.
- Knowledge of clinical trial data, systems, and global clinical operations.
- Experience working with diverse global stakeholders.
- Hands-on experience in a hospital or clinical trial site setup is preferred.
Required Skills
- Clinical Trials
- ICH-GCP
- Clinical Trial Data
- Clinical Operations
- Dose Surveillance
- Risk-Based Quality Management
- Data Analysis
- Clinical IT Systems
- Stakeholder Management
- Communication
- Problem Solving
- AI & Digital Tools
- Clinical Monitoring
How to Apply
Interested candidates can apply through the official Novo Nordisk careers page:
Conclusion
This Novo Nordisk job Bangalore opportunity offers a chance to contribute significantly to clinical research and patient safety through effective dose surveillance. Qualified candidates are encouraged to apply before the deadline of 20 October 2026.
