Novo Nordisk is hiring for the position of Dose Surveillance Advisor in Bangalore, Karnataka. The role is part of the Centralised Monitoring Unit (CMU), Research & Development, within Novo Global Business Services, India.
The position focuses on dose surveillance across global clinical trials, including identifying differences between prescribed and expected doses, following up with trial teams and sites, and maintaining inspection-ready records.
Job Details
| Details | Information |
|---|---|
| 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 |
Position
Dose Surveillance Advisor
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.
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 & Qualifications
- Postgraduate degree in Life Sciences.
- M.Pharm, PharmD, MDS or MSc Nursing are 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.
Application Details
