Dose Surveillance Advisor – Clinical Development Job At Novo Nordisk
Novo Nordisk is hiring a Dose Surveillance Advisor to support global clinical trials through centralized dose surveillance, risk identification, and protocol compliance. This Pharmacy Job role plays a critical part in ensuring patient safety, data integrity, and inspection-ready documentation across international clinical studies. Graduates seeking M Pharma jobs or PharmD Jobs can apply now.
Job Details
- Job Title: Dose Surveillance Advisor
- Location: Bangalore, Karnataka, India
About the Company
Novo Nordisk is a global healthcare leader focused on defeating serious chronic diseases. With over 100 years of innovation, the company combines science, technology, and purpose to improve patient outcomes worldwide while fostering an inclusive and collaborative work environment. This Pharmacy Job role plays a significant role in the company.
Educational Requirements
- Graduate degree in Life Sciences
(M-Pharma, PharmD) - Strong understanding of clinical trial conduct and ICH-GCP
Key Responsibilities
- Monitor adherence to prescribed dose status across assigned trial sites
- Identify and follow up on prescribed versus expected dose discrepancies
- Document dose-related operational risks in inspection-ready systems
- Perform routine and ad-hoc dose surveillance reviews per protocol
- Collaborate with Trial Managers, Clinical Medical Managers, and Medical Advisors
- Support site engagement through data insights and clear communication
- Coach site staff on dose compliance, documentation quality, and protocol adherence
- Communicate findings to trial squads and medical partners
- Contribute to continuous improvement and evolution of dose surveillance practices
Skills Required
- Strong knowledge of clinical trial operations and global clinical systems
- Excellent communication and stakeholder management skills
- Strong analytical and problem-solving abilities
- Ability to independently manage complex operational challenges
- High ownership, motivation, and continuous improvement mindset
- Capability to coach and influence site staff and cross-functional teams
Experience Required
- Minimum 2 years of experience in clinical trials
(Pharma, Biotech, CRO, or Hospital settings – mandatory) - Experience working with global and cross-functional stakeholders
About the Department
Novo Nordisk’s Centralized Monitoring Unit (CMU), Bangalore, focuses on Risk-Based Quality Management (RBQM). The team supports early identification and mitigation of risks impacting patient safety and data quality through centralized oversight and advanced monitoring methodologies. Graduates seeking M Pharma jobs or PharmD Jobs can apply now.
