Novo Nordisk is currently hiring a Dose Surveillance Advisor to join its Centralized Monitoring Unit (CMU) in Bangalore. This opportunity is ideal for professionals with clinical trial monitoring experience, RBQM knowledge, and ICH-GCP understanding.
The role focuses on dose surveillance, protocol compliance, patient safety monitoring, and clinical data oversight across global clinical trials. Candidates with experience in clinical research organizations (CROs), pharmaceutical companies, or hospital-based clinical trials are encouraged to apply.
Novo Nordiskโs Global Business Services (GBS) India team plays a critical role in supporting global clinical development operations and ensuring high-quality clinical trial data and regulatory compliance.
Job Details
| Field | Information |
|---|---|
| Position | Dose Surveillance Advisor |
| Department | Clinical Development โ Centralized Monitoring Unit |
| Company | Novo Nordisk |
| Job Location | Bangalore, India |
| Experience | Minimum 2 Years |
| Qualification | M.Pharm, PharmD, BDS, MDS, Pharmacy, MSc Nursing |
| Industry | Pharmaceutical / Clinical Research |
Key Responsibilities
The Dose Surveillance Advisor will support global clinical trials by ensuring protocol-compliant dosing and monitoring across trial sites.
Key responsibilities include:
- Monitor adherence to prescribed dose status across assigned clinical trial sites
- Identify dose discrepancies between prescribed vs expected doses
- Communicate with clinical trial sites and medical teams for corrective actions
- Maintain inspection-ready documentation of dose-related operational risks
- Conduct routine and ad-hoc dose surveillance reviews aligned with protocol requirements
- Collaborate with Clinical Medical Managers and Trial Managers
- Provide coaching and guidance to site staff on dose compliance and protocol adherence
- Deliver data insights and analytical findings to trial teams
- Support risk-based quality management (RBQM) initiatives and trial quality improvement
This role contributes directly to patient safety, trial integrity, and regulatory compliance in global clinical studies.
Eligibility Criteria
Education
Candidates must have a graduate degree in Life Sciences, including:
- M.Pharm
- PharmD
- BDS / MDS
- Pharmacy
- MSc Nursing
A strong understanding of clinical trial conduct and ICH-GCP guidelines is required.
Experience
Applicants should have:
- Minimum 2 years of clinical trial experience
- Experience in pharma, biotech, CRO, or hospital clinical research settings
- Familiarity with clinical trial data systems and global clinical operations
Required Skills
Successful candidates should demonstrate:
- Strong clinical data analysis and problem-solving ability
- Knowledge of risk-based monitoring (RBQM)
- Excellent communication and stakeholder management
- Ability to coach and influence clinical trial sites
- Strong analytical thinking and compliance mindset
About Novo Nordisk Centralized Monitoring Unit
Novo Nordiskโs Centralized Monitoring Unit (CMU) in Bangalore is a specialized team dedicated to risk-based quality management (RBQM) in clinical trials.
The team works closely with global trial teams and RBQM offices in Denmark, focusing on:
- Clinical data quality oversight
- Patient safety monitoring
- Risk detection and mitigation
- Central monitoring analytics
This multidisciplinary unit includes medical reviewers, statistical monitors, clinical data specialists, and monitoring experts, ensuring robust oversight of global clinical development programs.
Why Join Novo Nordisk
Working at Novo Nordisk provides opportunities to contribute to global healthcare innovation and chronic disease research.
Employees benefit from:
- Exposure to global clinical development programs
- Collaboration with international trial teams
- Career growth in clinical operations and centralized monitoring
- Work culture focused on innovation, diversity, and patient impact
With over 100 years of healthcare leadership, Novo Nordisk continues to pioneer solutions that improve lives worldwide.
How to Apply
