Novo Nordisk Global Business Services (GBS), India, is hiring for two critical roles in its Centralized Monitoring Unit (CMU), Bangalore:
- Dose Surveillance Advisor
- Senior Dose Surveillance Advisor
These roles are ideal for clinical research professionals passionate about patient safety, dose compliance, and risk-based quality management (RBQM) in global clinical trials. With Novo Nordisk’s strong legacy in defeating chronic diseases, this opportunity places you at the heart of data-driven clinical oversight and global trial excellence.
Open Positions (2 Roles)
1. Dose Surveillance Advisor – Clinical Development
Location: Bangalore, Karnataka
Experience Required: Minimum 2 years (mandatory)
2. Senior Dose Surveillance Advisor – Clinical Development
Location: Bangalore, Karnataka
Experience Required: Minimum 4 years (mandatory)
Key Responsibilities
Dose Surveillance Advisor
- Monitor adherence to prescribed dosing across assigned global trial sites
- Identify prescribed vs. expected dose discrepancies and ensure traceable follow-ups
- Collaborate with Clinical Medical Managers (CMMs) and Medical Advisors
- Document dose-related operational risks and maintain inspection-ready records
- Conduct routine and ad-hoc dose surveillance reviews per protocol
- Support trial teams with data insights, issue escalation, and site engagement
- Coach site staff on dose compliance, documentation quality, and protocol adherence
Senior Dose Surveillance Advisor
- Lead end-to-end dose surveillance across multiple trials (start-up to close-out)
- Perform advanced dose reviews and manage complex discrepancy resolutions
- Document risks in systems such as SPOT / COSMOS
- Drive audit and inspection readiness aligned with ICH-GCP and SOPs
- Provide data-driven insights to trial squads and global stakeholders
- Mentor junior team members and contribute to training initiatives
- Support innovation and continuous improvement in RBQM methodologies
Educational Qualifications
- Graduate degree in Life Sciences such as:
- M.Pharm / PharmD
- BDS / MDS
- Pharmacy
- MSc Nursing
- Strong understanding of clinical trial conduct and ICH-GCP guidelines
Skills & Competencies
- Strong analytical and problem-solving mindset
- Excellent communication and stakeholder management skills
- Hands-on experience with clinical trial data and IT systems
- Ability to work independently in a fast-evolving global environment
- High ownership, motivation, and continuous improvement mindset
- Coaching and influencing skills for site and team engagement
Why Join Novo Nordisk?
- Work in a global RBQM-driven clinical environment
- Exposure to international clinical trial operations
- Strong culture of inclusion, innovation, and purpose-driven work
- Opportunity to directly impact patient safety and data quality
- Long-term career growth in a world-leading pharmaceutical organization
Salary (Indicative – India)
- Dose Surveillance Advisor: ₹9,00,000 – ₹14,00,000 per annum
- Senior Dose Surveillance Advisor: ₹15,00,000 – ₹22,00,000 per annum
(Final compensation will be based on experience, skills, and internal benchmarks.)
How to Apply
Application Link For Dose Surveillance Advisor – Clinical Development
Application Link For Senior Dose Surveillance Advisor – Clinical Development
