Novo Nordisk Hiring 2026 – Dose Surveillance Advisor Job in Bangalore
Are you looking to build a career in clinical development, clinical trial monitoring and patient safety?
Novo Nordisk is hiring a Dose Surveillance Advisor for its Centralised Monitoring Unit within Research & Development in Bangalore, Karnataka.
The role is designed for professionals with 1–2 years of experience working with patient data in a hospital, clinical trial site, pharmaceutical, biotechnology or CRO environment.
Candidates with postgraduate qualifications in Life Sciences, particularly M.Pharm, PharmD, MDS or MSc Nursing, are preferred.
About Novo Nordisk
Novo Nordisk is a global healthcare company focused on developing solutions for people living with serious chronic diseases.
The company places strong emphasis on:
- Patient safety
- Clinical development
- Scientific innovation
- Regulatory compliance
- Data-driven monitoring
- Risk-Based Quality Management
Novo Nordisk’s operations in India support international clinical development activities and provide opportunities to work with global teams and modern clinical technologies.
Job Overview
| Job Details | Information |
|---|---|
| Company | Novo Nordisk |
| Position | Dose Surveillance Advisor |
| Department | Centralised Monitoring Unit, Research & Development |
| Experience | 1–2 Years |
| Qualification | Postgraduate degree in Life Sciences |
| Preferred Qualifications | M.Pharm / PharmD / MDS / MSc Nursing |
| Location | Bangalore, Karnataka |
| Work Type | Full-time, on-site |
Dose Surveillance Advisor – Role Overview
The Dose Surveillance Advisor will focus on dose compliance across clinical trial sites.
The position involves reviewing prescribed and expected doses, identifying potential deviations and coordinating follow-up with clinical trial sites and internal stakeholders.
The role also contributes to maintaining high-quality, inspection-ready clinical data while supporting patient safety and clinical trial quality.
Eligibility Criteria
Candidates should have:
- A postgraduate degree in Life Sciences
- 1–2 years of experience working with patient data
- Experience in a hospital, clinical trial site, pharmaceutical company, biotechnology company or CRO
- Knowledge of clinical trial conduct
- Understanding of ICH-GCP
- Familiarity with clinical trial data and systems
- Strong communication and stakeholder-management skills
Preferred Educational Background
- M.Pharm
- PharmD
- MDS
- MSc Nursing
Hands-on experience in a hospital or clinical trial site is preferred.
Skills Required
The ideal candidate should demonstrate:
- Clinical trial knowledge
- ICH-GCP understanding
- Clinical data familiarity
- Analytical thinking
- Problem-solving ability
- Strong communication skills
- Relationship-building skills
- Stakeholder influencing skills
- Ability to work with global teams
- Aptitude for clinical IT systems
- Familiarity with AI and digital tools
- Independent decision-making
- Adaptability and continuous learning
Candidates should also have a curious, accountable and results-oriented approach to their work.
Key Responsibilities
As a Dose Surveillance Advisor, the selected candidate will be responsible for:
- Overseeing prescribed dose compliance across assigned clinical trial sites
- Conducting routine and ad-hoc dose surveillance reviews according to study protocols
- Identifying differences between prescribed and expected doses
- Following up with clinical trial sites and relevant stakeholders
- Supporting sites through communication, data insights and escalation
- Collaborating with Trial Managers on dose and patient-retention matters
- Sharing surveillance findings with trial squads and medical partners
- Documenting dose-related operational risks
- Maintaining inspection-ready records
- Contributing to continuous improvement of the dose surveillance function
Role in Clinical Trial Quality
Dose compliance is an important aspect of clinical trial execution because deviations can affect study quality and patient safety.
In this role, professionals will work with clinical data and trial stakeholders to identify potential dose-related issues and ensure appropriate follow-up.
The position therefore combines clinical operations, data review, patient safety and stakeholder management.
Salary & Benefits
The supplied vacancy information does not specify a salary figure.
Potential professional benefits include:
- Career growth with a global healthcare organization
- Exposure to international clinical development
- Experience in data-driven monitoring
- Learning opportunities in Risk-Based Quality Management
- Exposure to AI and digital clinical tools
- Collaboration with international stakeholders
- Inclusive and quality-focused work environment
- Opportunity to contribute to patient-focused clinical trials
Candidates can confirm the complete compensation and benefits package during the recruitment process.
Application Deadline
Last Date to Apply: October 20, 2026
Interested candidates should submit their application before the stated deadline.
How to Apply
Eligible candidates should apply directly through the official Novo Nordisk Careers portal.
Position
Dose Surveillance Advisor
Location
Bangalore, Karnataka, India
Applicants should highlight the following in their resume:
- Postgraduate Life Sciences qualification
- Patient-data experience
- Clinical trial or hospital experience
- ICH-GCP knowledge
- Clinical data and systems exposure
- Stakeholder-management experience
Official Application
Candidates should use the official Novo Nordisk Careers website and search for the Dose Surveillance Advisor position in Bangalore.
Applicants are advised to verify the current vacancy status and application deadline directly on the official careers portal before submitting their application.
Verified Job Information
The supplied vacancy identifies this as a verified post and provides an official Novo Nordisk career listing for the Dose Surveillance Advisor position.
Candidates should use the official careers portal for the application rather than relying on third-party application links.
Why Join Novo Nordisk?
This opportunity can be a strong fit for Life Sciences professionals who want to move into clinical development and centralized monitoring.
The position provides exposure to:
- Global clinical trials
- Patient safety
- Clinical data surveillance
- Risk-Based Quality Management
- International clinical operations
- Digital and AI-enabled tools
- Cross-functional collaboration
Professionals can also develop their expertise in clinical operations while contributing to the quality and safety of clinical research programs.
Frequently Asked Questions
1. Who can apply for the Novo Nordisk Dose Surveillance Advisor role?
Candidates with a postgraduate degree in Life Sciences and 1–2 years of patient-data experience in relevant clinical or research environments can apply.
2. What qualifications are preferred?
M.Pharm, PharmD, MDS and MSc Nursing are specifically preferred in the supplied vacancy information.
3. Is clinical or hospital experience required?
Experience working with patient data in a hospital, clinical trial site, pharma, biotech or CRO setting is required. Hands-on hospital or clinical trial site experience is preferred.
4. What is the job location?
The position is based in Bangalore, Karnataka, India.
5. What is the application deadline?
The supplied vacancy states that applications should be submitted before October 20, 2026.
6. What clinical knowledge is required?
Candidates should have knowledge of clinical trial conduct and ICH-GCP, along with familiarity with clinical data and systems.
7. What does a Dose Surveillance Advisor do?
The role focuses on reviewing dose compliance across clinical trial sites, identifying potential deviations, coordinating follow-up and documenting dose-related operational risks.
8. Is this a remote position?
The supplied job details describe the position as full-time, with the work location in Bangalore. The source does not identify it as a remote role.
