Company: Novo Nordisk
Job Role: Medical Reviewer
Department: Central Monitoring Unit (CMU) – Clinical Drug Development
Location: Bengaluru, Karnataka, India
Job Category: Clinical Development
Experience Required: 2–5 Years
Eligibility: MBBS + MD
Job Type: Full-Time
Application Deadline: 8th May 2026
Freshers Eligible: No
About the Company
Novo Nordisk is one of the world’s leading healthcare organizations dedicated to defeating serious chronic diseases through innovation, research, and patient-centric healthcare solutions. With more than 100 years of global excellence, Novo Nordisk continues to transform healthcare through advanced clinical research, scientific innovation, and cutting-edge drug development programs.
The company’s Global Business Services (GBS) division in Bengaluru plays a strategic role in supporting worldwide clinical development and centralized monitoring operations.
Job Overview – Medical Reviewer
Novo Nordisk is hiring experienced Medical Review professionals for its Centralized Monitoring Unit (CMU) in Bangalore. This role focuses on ensuring patient safety, maintaining high-quality clinical trial data, and supporting medical oversight activities across global clinical development programs.
Please Note: This is a Clinical Development and Medical Review role and not a Pharmacovigilance position.
The selected candidate will collaborate with global study teams, medical specialists, data managers, and trial managers to perform comprehensive medical review activities aligned with ICH-GCP guidelines, protocol compliance standards, and regulatory requirements.
Key Responsibilities
Perform detailed medical review of clinical trial subjects to ensure data consistency, integrity, and patient safety
Ensure adherence to study protocols, ICH-GCP guidelines, SOPs, and local regulatory requirements
Collaborate with Trial Managers, Data Managers, and Medical Specialists during clinical trial execution
Identify, escalate, and help resolve medical inconsistencies and clinically significant findings within trial data
Participate in medical review planning activities and contribute to Medical Monitoring Plans (MMPs)
Review medical monitoring displays, data listings, and clinical datasets for effective risk-based monitoring
Present medical review findings to Medical Specialists to support informed clinical decision-making
Document medical review activities within Sponsor Trial Master File (TMF) systems
Support protocol compliance monitoring and medical data cleaning activities
Ensure timely communication of medical review status according to project communication and blinding plans
Required Qualifications
Candidates applying for this Clinical Research and Medical Review job in Bangalore should meet the following requirements:
MBBS + MD qualification from a recognized institution
2–5 years of relevant experience in Medical Review, Clinical Development, or Clinical Research
Strong knowledge of ICH-GCP guidelines and clinical trial processes
Excellent understanding of medical terminology and clinical trial activities
Experience with risk-based monitoring methodologies
Familiarity with clinical trial data systems, medical monitoring tools, and operational dashboards
Strong analytical, communication, and stakeholder management skills
Proficiency in MS Office, PowerPoint, and related clinical documentation tools
Excellent written and verbal English communication skills
About the Centralized Monitoring Unit (CMU)
The Centralized Monitoring Unit (CMU) at Novo Nordisk Bengaluru is a highly specialized division within Clinical Drug Development. The department combines medical expertise with advanced technical and analytical capabilities to strengthen clinical trial oversight and patient safety monitoring.
Medical reviewers work closely with global medical specialists, particularly teams based in Denmark, to support:
Risk-based medical monitoring
Protocol compliance reviews
Identification of clinically significant outliers
Medical data cleaning and validation
Detection of unusual data trends and systematic errors
Centralized clinical trial monitoring activities
The department also leverages advanced visualization tools and statistical monitoring systems to improve clinical trial quality and operational excellence.
Why Join Novo Nordisk?
Working at Novo Nordisk offers professionals an opportunity to contribute to life-changing healthcare innovations while building a strong global clinical research career.
Key benefits include:
Exposure to global clinical development programs
Collaborative international work environment
Opportunities to work with advanced clinical technologies and monitoring systems
Strong focus on employee growth, inclusion, and innovation
Career advancement in Clinical Research and Medical Monitoring domains
Important Note for Applicants
This role is designed for experienced medical professionals with prior exposure to clinical development and medical review activities. Freshers and entry-level candidates are not eligible for this position.
Candidates interested in entering the Clinical Research or Pharmacovigilance industry may explore beginner roles such as:
Clinical Research Coordinator (CRC)
Drug Safety Associate
Clinical Data Associate
Medical Writer
Pharmacovigilance Associate
How to Apply
Interested candidates can apply through the official careers portal of Novo Nordisk before the application deadline.
For more verified Clinical Research, Pharmacovigilance, Medical Review, Regulatory Affairs, and Healthcare jobs worldwide, visit ThePharmaDaily.com.
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