Dose Surveillance Advisor Recruitment at Novo Nordisk Bangalore
Novo Nordisk has announced an opening for the position of Dose Surveillance Advisor at its Global Business Services (GBS) centre in Bangalore, Karnataka, India. This clinical development role is ideal for candidates with experience in clinical trial data surveillance and protocol compliance. The post is based on the official job posting from Novo Nordisk’s careers portal.
Novo Nordisk Company Overview
Novo Nordisk is a global healthcare company focused on improving outcomes for patients with chronic diseases. The Centralized Monitoring Unit (CMU) in Bangalore supports global clinical trial quality and data risk management activities.
Novo Nordisk Post Name & Vacancy Details
Role: Dose Surveillance Advisor
Department
Centralized Monitoring Unit, Novo Nordisk Global Business Services (GBS), Bangalore
Location
Bangalore, Karnataka, India
Job Category
Clinical Development
Eligibility Criteria for Dose Surveillance Advisor
- Graduate degree in Life Sciences such as M-Pharm, PharmD, BDS/MDS, Pharmacy, MSc Nursing, or equivalent with strong clinical trial knowledge.
- Minimum 2 years of relevant experience in clinical trials within pharma/biotech/CRO/hospital settings.
- Familiarity with ICH-GCP guidelines and clinical operations standards.
Dose Surveillance Advisor Key Responsibilities
- Oversee adherence to prescribed dose status across assigned trial sites.
- Identify and manage discrepancies between prescribed and expected dose metrics.
- Document dose-related operational risks and maintain inspection-ready records.
- Support site engagement, clear communication, and escalation of issues to drive trial quality.
- Execute routine and ad-hoc dose surveillance reviews per protocol requirements.
- Coach site staff to strengthen compliance and documentation practices.
How to Apply Novo Nordisk
Candidates should apply online through the official Novo Nordisk careers portal. Click the “Apply now” button below to submit your CV and required documents via the official application page.
Important Dates
Read the official job posting carefully for closing dates and application timelines. No dates are explicitly provided in the official source.
Selection Process
Selection is based on the company’s recruitment procedures and may include application screening, skill assessments, and interviews. No guarantees of selection are provided here.
Frequently Asked Questions
What is the educational requirement for this role?
A graduate degree in Life Sciences (e.g., M-Pharm, PharmD, Pharmacy, MSc Nursing) with clinical trial knowledge.
Where is the Dose Surveillance Advisor position based?
The role is located at Novo Nordisk’s Bangalore, Karnataka, India office.
How many years of experience are expected?
Minimum 2 years of relevant clinical trial experience.
