Senior Medical Reviewer – Clinical Development | Bangalore, India
Company: Novo Nordisk Global Business Services (GBS), India
Location: Bangalore, Karnataka, India
Employment Type: Full-Time, Permanent
Department: Centralized Monitoring Unit (CMU) – Clinical Development
Experience Required: 5+ Years
Application Deadline: 15th January 2026
Job Overview
Novo Nordisk GBS is seeking a highly skilled Senior Medical Reviewer to join the Centralized Monitoring Unit (CMU) in Bangalore. This role focuses on medical oversight in clinical drug development, ensuring the quality, consistency, and integrity of clinical trial data. Please note, this position is not a Pharmacovigilance role.
The ideal candidate will have a strong background in clinical trials, risk-based monitoring, and medical data review, along with excellent stakeholder communication and analytical skills.
Key Responsibilities
Conduct comprehensive medical reviews of clinical trial data to ensure patient safety, protocol compliance, and adherence to regulatory standards (ICH-GCP)
Collaborate closely with Data Managers, Trial Managers, and Medical Specialists to maintain high-quality clinical deliverables
Identify, analyze, and resolve medical concerns or inconsistencies in clinical data in collaboration with investigational site staff and healthcare professionals
Present findings of medical reviews to relevant medical specialists for informed decision-making
Document medical review activities in the Trial Master File (TMF) ensuring inspection readiness
Perform quality control of medical review tasks, ensuring accuracy and regulatory compliance
Train and mentor new team members, providing therapeutic area guidance, process training, and best practice sharing
Plan and manage resources for medical review tasks, including timeline planning and workload allocation
Contribute to process improvement initiatives and shared team objectives
Required Qualifications & Experience
Education: MBBS + MD (or equivalent)
Experience: Minimum 5 years in clinical trial medical review or clinical development oversight
Strong knowledge of ICH-GCP guidelines and clinical trial processes
Proficiency in MS Office, MS Project, and PowerPoint
Familiarity with clinical trial data systems, risk-based monitoring methodologies, and medical terminology
Excellent analytical, communication, and stakeholder management skills
Ability to handle complex tasks independently and provide results-oriented solutions
About the Department
The Centralized Monitoring Unit (CMU) in Bangalore is integral to Novo Nordisk’s clinical development operations. CMU focuses on risk-based medical monitoring, data cleaning, protocol compliance, and identification of clinically significant outliers. Medical reviewers work alongside medical specialists in Denmark and statistical programmers to ensure patient safety and high-quality clinical data outputs.
Working at Novo Nordisk
Novo Nordisk is a global leader in healthcare, committed to defeating serious chronic diseases and promoting long-term health. Our culture values innovation, collaboration, and a patient-first mindset. We focus on scientific excellence, accessibility of healthcare, and sustainable solutions that improve millions of lives worldwide.
Diversity & Inclusion: Novo Nordisk promotes an inclusive workplace and equality of opportunity for all applicants.
Fraud Notice: Novo Nordisk does not charge candidates fees or request payments for employment. Be aware of fraudulent job offers.
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