Medical Reviewer Job at Novo Nordisk in Bangalore
The Medical Reviewer Job at Novo Nordisk is a valuable opportunity for qualified medical professionals seeking to grow their careers in clinical development. This role, based in Bangalore, is ideal for candidates looking to build a long-term Novo Nordisk career while contributing to patient safety, medical monitoring, and high-quality clinical trial outcomes.
Medical Reviewer Job Details:
- Job Title: Associate Medical Reviewer
- Location: Bangalore, India
- Job Category: Clinical Development
- Department: Central Monitoring Unit, GBS Bengaluru
- Location: Bengaluru, India
- Deadline: 15th January 2026.
About the Company
Novo Nordisk is a global healthcare company with more than 100 years of experience in addressing serious chronic diseases. Known for its innovative mindset and strong ethical foundation, the organization offers meaningful growth through a global Novo Nordisk career pathway. Novo Nordisk Global Business Services (GBS) in India supports worldwide clinical drug development with high-quality medical and operational expertise.
Qualifications
- MBBS + MD qualification
- 1–2 years of experience in clinical practice or academics
- Strong knowledge of ICH GCP guidelines
- Excellent understanding of medical terminology and clinical trial processes
- Experience with risk-based monitoring methodologies
- Familiarity with clinical trial data systems and tools
- Proficiency in MS Office, MS Project, and PowerPoint
- Strong written and spoken English skills
- Analytical, result-oriented mindset with independent task management ability
- Effective communication and stakeholder management skills
Medical Reviewer Job Description
This Medical Reviewer Job involves conducting medical reviews of trial subjects across assigned clinical trials to ensure high-quality, consistent medical data. The role emphasizes patient safety and compliance with protocols, Good Clinical Practice (GCP), ICH guidelines, local regulations, and standard operating procedures.
Key Responsibilities
- Perform medical review of clinical trial subjects to ensure data accuracy
- Ensure patient safety and compliance with GCP, ICH guidelines, and SOPs
- Identify clinically significant outliers and inconsistencies in trial data
- Collaborate with site staff, healthcare professionals, and trial teams
- Present medical review findings to Medical Specialists
- Conduct protocol compliance checks and medical monitoring activities
- Maintain documentation to support inspection readiness
- Continuously update therapeutic and protocol-specific knowledge
