Novo Nordisk, a global leader in diabetes care and clinical innovation, has announced multiple hiring opportunities in Bengaluru across medical review, centralized monitoring, statistical monitoring, and clinical data analytics functions. These roles support global clinical trials and align with ICH-GCP, RBQM, and regulatory compliance standards.
This recruitment drive is ideal for MBBS/MD professionals, clinical research experts, CRAs, data managers, and life-science graduates looking to advance their careers with a top multinational pharmaceutical company.
📌 Open Positions at Novo Nordisk (Bengaluru)
1️⃣ Senior Medical Reviewer (5–10 Years)
Key Responsibilities
- Conduct end-to-end medical review of clinical trial data
- Ensure patient safety, protocol compliance, and regulatory adherence
- Document reviews in Trial Master File (TMF) and ensure inspection readiness
- Mentor junior reviewers and support resource planning
Qualifications
- MBBS + MD with 5+ years of experience
- Strong knowledge of ICH-GCP and clinical trial systems
- Experience in risk-based monitoring and medical data review
2️⃣ Medical Reviewer Professional (2–5 Years)
Key Responsibilities
- Perform medical review of all trial subjects
- Collaborate with Data Managers, Trial Managers, and Medical Specialists
- Resolve medical inconsistencies with investigational sites
- Contribute to trial planning and medical monitoring activities
Qualifications
- MBBS + MD with 2–5 years of experience
- Good understanding of GCP, ICH guidelines, and clinical data flow
3️⃣ Senior Functional Programmer (6–11 Years)
Key Responsibilities
- Develop RBQM dashboards and trial monitoring reports
- Use SAS, SQL, Python, Power BI, Qlik Sense, and JMP Clinical
- Lead stakeholder meetings and mentor programmers
- Ensure GxP compliance and system validation
Qualifications
- Bachelor’s/Master’s in Life Sciences, IT, or Computer Science
- 4+ years in clinical data management or bioinformatics
- Advanced programming and clinical data systems expertise
4️⃣ Associate Statistical Monitor (0–2 Years)
Key Responsibilities
- Perform statistical monitoring to detect data anomalies and risks
- Analyze clinical trial data and support quality improvement
- Collaborate with project teams and support training initiatives
Qualifications
- Degree in Life Sciences or Engineering
- Exposure to SAS JMP and basic statistical methods
- Understanding of GCP and clinical research processes
5️⃣ Central Monitor Professional (3–8 Years)
Key Responsibilities
- Define and monitor Key Risk Indicators (KRIs)
- Perform centralized monitoring using RBQM principles
- Use data visualization tools for operational risk detection
- Communicate findings to cross-functional stakeholders
Qualifications
- Bachelor’s degree in Life Sciences or Healthcare
- 3+ years of clinical research experience
- Experience in centralized monitoring or CRA roles preferred
6️⃣ Senior Central Monitor Professional (5–10 Years)
Key Responsibilities
- Lead centralized monitoring strategies and RBQM implementation
- Design advanced analytics and AI-enabled monitoring approaches
- Mentor teams and support audits and inspections
- Drive process optimization and innovation
Qualifications
- Bachelor’s degree in Life Sciences or Healthcare
- 5+ years of clinical research and RBQM experience
- Strong exposure to GCP E6 (R2/R3), analytics, and digital tools
🎯 Why Join Novo Nordisk?
- Work on global clinical trials with cutting-edge methodologies
- Strong focus on patient safety, data integrity, and innovation
- Competitive compensation and long-term career growth
- Exposure to RBQM, AI-driven monitoring, and global regulatory standards
📝 How to Apply
Application Link for Senior Medical Reviewer
Application Link for Medical Reviewer Professional
Application Link for Senior Functional Programmer
Application Link for Associate Statistical Monitor
Application Link for Central Monitor Professional
Application Link for Senior Central Monitor Professional
