Associate Medical Reviewer Job | Novo Nordisk Hiring

Novo Nordisk is a global healthcare leader with over 100 years of innovation in defeating chronic diseases like diabetes, obesity, and rare blood disorders. With a presence in 170+ countries, we impact 40+ million patients daily. Our 72,000+ employees drive change through cutting-edge research, patient-centric care, and sustainable practices.

Job Description: Associate Medical Reviewer

Department: Centralised Monitoring Unit (CMU)

The CMU combines medical expertise & data analytics to ensure patient safety & trial integrity. The team includes:

• Medical Reviewers (ensuring compliance & patient safety)
• Functional Programmers (developing data visualization tools)
• Statistical Monitors (detecting data anomalies & fraud)

Key Responsibilities:

✔ Conduct medical reviews of clinical trial data across therapy areas.
✔ Ensure protocol adherence, GCP, ICH guidelines, and SOP compliance.
✔ Collaborate with Data Managers, Trial Managers & Medical Specialists.
✔ Escalate safety concerns and document findings in Trial Master File (TMF).
✔ Train new team members on medical review processes.
✔ Contribute to Medical Monitoring Plans (MMP) & data listings.

Eligibility & Qualifications

Must-Have:

🎓 MBBS or MD (any clinical specialty).
💼 1+ years in clinical research (medical monitoring, safety surveillance, or drug development).
📊 1-2 years of project management experience.
💻 Proficiency in MS Office, MS Project, PowerPoint.
🌍 Fluent in English (written & spoken).

Preferred:

🔍 Experience in risk-based monitoring (RBM).
📈 Knowledge of data visualization tools (e.g., Spotfire, Tableau).

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