Novo Nordisk is a global healthcare leader with a 100-year legacy of combating chronic diseases. Known for pioneering diabetes care, the company now impacts over 40 million patients worldwide daily. With a workforce of 72,000+ employees, Novo Nordisk fosters innovation, collaboration, and professional growth. Ranked among the top 20 most valuable companies by market cap, Novo Nordisk offers a dynamic work environment where employees drive meaningful change in global healthcare.
Job Description: Senior Medical Reviewer
Key Responsibilities:
- Conduct medical reviews of clinical trial data across multiple therapy areas.
- Ensure patient safety, protocol compliance, and data integrity following GCP, ICH guidelines, and SOPs.
- Collaborate with Data Managers, Trial Managers, and Medical Specialists to resolve data inconsistencies.
- Present medical review findings to Medical Specialists for decision-making.
- Contribute to trial planning, risk-based monitoring, and medical data cleaning.
- Provide training and mentorship to new team members.
- Review and provide inputs on Medical Monitoring Plans (MMP) and data visualization tools.
Qualifications & Experience:
- MBBS + MD (Pharmacology preferred) or related clinical/paraclinical fields.
- 3-5 years in Clinical Drug Development (Medical Review, Monitoring, Safety Surveillance, or Clinical Research).
- 1-2 years of project management experience is required.
- Strong knowledge of ICH-GCP, medical terminology, and clinical trial processes.
- Proficiency in MS Office, MS Project, and data analysis tools.
- Excellent analytical, communication, and English proficiency skills.
Why Join Novo Nordisk?
✅ Work in a globally recognized healthcare leader.
✅ Engage in cutting-edge clinical research with real-world impact.
✅ Collaborative, inclusive, and growth-oriented work culture.
✅ Opportunity to contribute to life-changing therapies.
