Location: Bangalore, Karnataka, India
Department: Central Monitoring Unit (CMU), Global Business Services
Company: Novo Nordisk
Application Deadline: 8th May 2026
Experience Required: 2–5 years (Not suitable for freshers)
About the Role
Novo Nordisk is hiring a Medical Reviewer for its Centralised Monitoring Unit in Bengaluru. This role is designed for professionals passionate about clinical research, patient safety, and medical data integrity.
This is a clinical development role focused on medical review and not a pharmacovigilance position. The selected candidate will provide medical oversight across clinical trials, ensuring compliance with global regulatory standards and maintaining the highest quality of clinical data.
Key Responsibilities
Perform comprehensive medical review of clinical trial data for all assigned studies
Ensure patient safety, protocol adherence, and compliance with ICH-GCP, SOPs, and regulatory guidelines
Identify data inconsistencies, clinically significant findings, and potential risks during trial conduct
Collaborate closely with Data Managers, Trial Managers, and Medical Specialists for effective trial execution
Generate and communicate medical review findings to support clinical decision-making
Participate in trial planning activities related to medical monitoring and review strategies
Contribute to Medical Monitoring Plans (MMP) and data visualization requirements
Escalate medical concerns and ensure timely resolution of issues with investigational sites
Document all medical review activities in Trial Master File (TMF) as per compliance requirements
Required Qualifications
MBBS with MD (mandatory)
2 to 5 years of experience in clinical research, medical review, or clinical development
Strong knowledge of ICH-GCP guidelines and regulatory frameworks
Proficiency in MS Office tools including PowerPoint and MS Project
In-depth understanding of medical terminology and clinical trial processes
Experience with risk-based monitoring methodologies
Familiarity with clinical trial data systems and analytical tools
Excellent communication, analytical, and stakeholder management skills
Ability to manage complex tasks independently and deliver within timelines
About the Department
The Centralised Monitoring Unit (CMU) in Bengaluru plays a strategic role in clinical drug development at Novo Nordisk. The team comprises medical experts, statisticians, and programmers working collaboratively to ensure high-quality, risk-based clinical monitoring.
Medical Reviewers work closely with global medical specialists, particularly from Denmark, to safeguard patient safety and ensure data accuracy. The department emphasizes advanced monitoring techniques, data visualization, and proactive risk identification across clinical trials.
Why Join Novo Nordisk
At Novo Nordisk, innovation is driven by purpose. With over 100 years of legacy in combating chronic diseases, the organization offers a unique environment where science, collaboration, and curiosity converge to create meaningful healthcare impact.
Employees benefit from:
A global, innovation-driven work culture
Opportunities to work on cutting-edge clinical development programs
Strong focus on diversity, inclusion, and career growth
A purpose-led mission to improve patient lives worldwide
Important Note for Applicants
This role requires prior experience in clinical development and medical review. Freshers are advised to explore entry-level roles such as Clinical Research Coordinator, Clinical Data Associate, or Pharmacovigilance Associate before progressing to Medical Reviewer positions.
How to Apply
Apply through the official careers page of Novo Nordisk or explore verified global job opportunities on ThePharmaDaily.com.
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