Associate Medical Reviewer

Department : Central Monitoring Unit, GBS Bengaluru
Location: Bengaluru, India
Novo Nordisk Global Business Services (GBS), India
Are you passionate about ensuring patient safety and high:quality clinical trial data? Do you want to play a key role in medical monitoring and contribute to improving lives through clinical research? If yes, we are looking for a dedicated Medical Reviewer to join our team in Bangalore. Read on and apply today
The Position
As an Associate Medical Reviewer, you will:
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Conduct medical review of all trial subjects in assigned clinical trials to ensure high:quality, consistent medical data. Ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and SOPs.
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Identify and resolve issues of medical concern or inconsistencies in clinical trial data by collaborating with investigational site staff and healthcare professionals.
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Present findings from medical reviews to relevant Medical Specialists to enable informed decision:making. Perform medical monitoring tasks, including protocol compliance checks, identifying clinically significant outliers, and ensuring data consistency.
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Document all medical review activities to always ensure inspection readiness.
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Stay updated on therapeutic knowledge, protocol:specific guidelines, and the latest medical developments. Collaborate closely with trial teams, including Data Managers, Trial Managers, and Medical Specialists, to ensure quality deliverables.
Qualifications
We are looking for a candidate with the following qualifications:
Need to have: :
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A graduate degree in MBBS MD with : 1:2 years of experience in clinical practice or academics
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Good knowledge of ICH GCP guidelines.
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Demonstrated computer skills (MS Office, MS Project, PowerPoint).
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Excellent understanding of medical terminology and clinical trial activities, Experience with risk:based monitoring methodologies. : Familiarity with clinical trial data systems and tools.
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Excellent written and spoken English, Strong analytical and result:oriented skills, Ability to plan and handle complex tasks independently, good communication and stakeholder management skills
About the department
The Centralized Monitoring Unit (CMU) in Bangalore is part of the Clinical Drug Development area. Our department is a perfect blend of skilled medical professionals (Medical Reviewers) and technical experts (Functional Programmers and Statistical Monitors). Medical Reviewers collaborate with Medical Specialists from Denmark to ensure patient safety and well:being in clinical trials by focusing on protocol compliance, identifying clinically significant outliers, and performing medical data cleaning. Functional Programmers develop operational visualizations to support proactive centralized monitoring, while Statistical Monitors detect unusual data patterns, systematic errors, and potential compliance issues. Join our dynamic and collaborative team to make a meaningful impact on clinical trial outcomes.
Working at Novo Nordisk
Every day we seek the solutions that defeat serious chronic diseases. To do this, we approach our work with an unconventional spirit, a rare determination, and a constant curiosity. For over 100 years, this unordinary mindset has seen us build a company unlike any other. One where a collective passion for our purpose, mutual respect, and a willingness to go beyond what we know delivers extraordinary results.
Deadline
15th January 2026
Disclaimer
It has been brought to our attention that there have recently been instances of fraudulent job offers, purporting to be from Novo Nordisk and/or its affiliate companies. The individuals or organisations sending these false employment offers may pose as a Novo Nordisk recruiter or representative and request personal information, purcha
Job Type: Permanent