Senior Medical Reviewer – Clinical Development
Category: Clinical Development
Job Type: Full-time
Department: Central Monitoring Unit (CMU), Global Business Services (GBS)
Location: Bangalore, Karnataka, India
Job Overview
Novo Nordisk is hiring an experienced Senior Medical Reviewer to join its Central Monitoring Unit (CMU) within Global Business Services, Bengaluru. This role is critical to ensuring patient safety, data integrity, and regulatory compliance across global clinical trials. The position offers an opportunity to work closely with international medical experts and contribute to high-quality clinical drug development activities.
Note: This role involves medical oversight in clinical drug development and is not a Pharmacovigilance position.
Key Responsibilities
Perform comprehensive medical reviews of clinical trial data to ensure patient safety, protocol compliance, and adherence to regulatory standards
Collaborate with cross-functional teams including Data Managers, Trial Managers, Medical Specialists, and study group members to deliver high-quality outcomes
Identify, investigate, and resolve medical inconsistencies and safety-related issues in collaboration with investigational sites and healthcare professionals
Present medical review findings to Medical Specialists to support informed clinical and safety decisions
Document medical review activities within the Sponsor Trial Master File (TMF) and maintain inspection readiness at all times
Conduct quality control checks on medical review outputs and ensure consistency across trials
Provide training, mentoring, and therapeutic area guidance to new team members
Contribute to process improvements, best practices, and continuous quality enhancement initiatives
Plan and manage medical review resources, timelines, and workload allocation effectively
Required Qualifications and Experience
MBBS with MD qualification
Minimum 5+ years of experience in medical review, clinical research, or clinical drug development
Strong working knowledge of ICH-GCP guidelines and global clinical trial regulations
Solid understanding of medical terminology, clinical trial processes, and risk-based monitoring methodologies
Experience with clinical trial data systems and monitoring tools
Proficiency in MS Office applications including Word, Excel, PowerPoint, and MS Project
Excellent written and spoken English communication skills
Strong analytical, problem-solving, and result-oriented mindset
Proven ability to manage complex tasks independently and engage effectively with multiple stakeholders
About the Department
The Centralised Monitoring Unit (CMU) in Bengaluru is an integral part of Novo Nordisk’s Clinical Drug Development function. The team comprises experienced medical reviewers, statistical monitors, and technical programmers who collaborate closely with global medical specialists, particularly from Denmark. CMU focuses on risk-based medical monitoring, protocol compliance, identification of clinically relevant data trends, and proactive medical data cleaning to ensure patient safety and trial excellence.
Why Join Novo Nordisk
Novo Nordisk is a global healthcare leader dedicated to addressing serious chronic diseases through science-driven innovation. With over a century of impact, the organization fosters a culture of curiosity, collaboration, and purpose, empowering employees to create meaningful and lasting improvements in global health outcomes.
Application Deadline
15 January 2026
Important Notice
Novo Nordisk does not charge any fees or request financial transactions at any stage of the recruitment process. Candidates are advised to remain cautious of fraudulent job offers.
Equal Opportunity Statement
Novo Nordisk is committed to an inclusive recruitment process and equal employment opportunities for all applicants, regardless of background.
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