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).
