Company: Novo Nordisk
Job Role: Associate Medical Reviewer
Department: Central Monitoring Unit (CMU) – Clinical Development
Location: Bengaluru, Karnataka, India
Job Category: Clinical Development / Medical Monitoring / Clinical Research
Experience Required: 1–2 Years Experience (Freshers Not Eligible)
Educational Qualification: MBBS + MD
Application Deadline: 8th May 2026
About the Company
Novo Nordisk is one of the world’s leading healthcare organizations focused on defeating chronic diseases through innovation, clinical research, and patient-centric healthcare solutions. With more than 100 years of global healthcare excellence, Novo Nordisk continues to drive advancements in diabetes care, obesity management, and rare disease treatment.
The company’s Global Business Services (GBS) division in Bengaluru plays a crucial role in supporting international clinical development and centralized medical monitoring activities.
Job Overview – Associate Medical Reviewer
Novo Nordisk is hiring skilled medical professionals for the role of Associate Medical Reviewer in Bengaluru. This opportunity is ideal for candidates with clinical or academic medical experience who are passionate about patient safety, clinical trial quality, medical monitoring, and regulatory compliance in global clinical research programs.
The selected candidate will work closely with Medical Specialists, Data Managers, Trial Managers, and Clinical Development teams to ensure high-quality clinical trial data review and protocol adherence.
Key Responsibilities
Conduct comprehensive medical review of clinical trial subjects across assigned studies
Ensure patient safety, protocol compliance, and adherence to ICH-GCP guidelines, SOPs, and local regulations
Identify clinically significant outliers, inconsistencies, and medical concerns in trial data
Collaborate with investigators, site staff, and healthcare professionals to resolve medical review issues
Perform medical monitoring activities and support centralized monitoring initiatives
Present medical review findings to Medical Specialists for informed clinical decision-making
Maintain accurate documentation to ensure inspection readiness and audit compliance
Support clinical data quality management and medical data cleaning activities
Stay updated with therapeutic area knowledge, protocol guidelines, and emerging medical developments
Work cross-functionally with Clinical Trial Teams, Data Management, and Monitoring Units
Required Qualifications
Mandatory Requirements
MBBS + MD qualification from a recognized institution
1–2 years of experience in clinical practice, academics, or clinical research
Strong understanding of ICH-GCP guidelines and clinical trial processes
Knowledge of medical terminology, clinical data review, and protocol compliance
Familiarity with risk-based monitoring methodologies and centralized monitoring activities
Experience using MS Office, PowerPoint, and clinical trial systems/tools
Excellent written and verbal communication skills in English
Strong analytical thinking and stakeholder management capabilities
Ability to independently manage complex clinical review tasks
About the Central Monitoring Unit (CMU)
The Central Monitoring Unit (CMU) at Novo Nordisk Bengaluru is a specialized division within Clinical Drug Development. The department combines the expertise of Medical Reviewers, Functional Programmers, and Statistical Monitors to ensure proactive clinical trial oversight and patient safety.
Medical Reviewers collaborate closely with global Medical Specialists from Denmark to identify protocol deviations, perform medical data cleaning, and monitor patient safety signals. The team also leverages operational visualizations and statistical monitoring methodologies to detect unusual data patterns and compliance risks across global studies.
Why Join Novo Nordisk?
Opportunity to work with a globally recognized pharmaceutical leader
Exposure to international clinical development programs and medical monitoring operations
Collaborative and innovation-driven work environment
Strong career growth opportunities in clinical research and medical affairs
Contribute directly to improving global patient outcomes and healthcare innovation
Important Note for Applicants
This position is not suitable for freshers. Candidates must possess an MBBS + MD qualification along with 1–2 years of relevant clinical, academic, or clinical research experience.
Professionals aspiring to build careers in Clinical Research, Medical Monitoring, Pharmacovigilance, Clinical Data Review, or Drug Development are encouraged to apply.
How to Apply
Eligible candidates can apply through the official careers portal of Novo Nordisk before the application deadline.
For more verified global Clinical Research, Pharmacovigilance, Medical Affairs, and Healthcare jobs, visit ThePharmaDaily.com.
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