Job Title: Senior Medical Reviewer
Category: Clinical Development
Location: Bangalore, Karnataka, India
Department: Central Monitoring Unit (CMU), Novo Nordisk Global Business Services (GBS), Bengaluru
Application Deadline: 15th January 2026
Novo Nordisk GBS India is seeking an experienced Senior Medical Reviewer to join our Centralized Monitoring Unit (CMU) in Bangalore. This role is critical for ensuring patient safety and maintaining the integrity of clinical trial data. The position focuses on medical oversight of clinical drug development, distinct from Pharmacovigilance activities.
As a Senior Medical Reviewer, you will be responsible for reviewing clinical trial data across multiple studies, ensuring compliance with protocols, ICH-GCP guidelines, local regulations, and internal SOPs. Your work will directly impact patient safety, clinical data quality, and trial success.
Conduct thorough medical review of all assigned trial subjects across multiple clinical trials.
Ensure adherence to Good Clinical Practice (GCP), ICH guidelines, local regulations, and SOPs.
Collaborate closely with Data Managers, Trial Managers, and Medical Specialists during trial conduct.
Document medical review findings in the Trial Master File (TMF) and report status per project communication and blinding plans.
Participate in trial planning and provide input on medical review processes, displays, and data listings.
Identify, clarify, and resolve medical inconsistencies or safety concerns with investigational sites.
Present medical review findings to relevant medical specialists to support informed decision-making.
Contribute to the development and refinement of risk-based medical monitoring strategies.
Educational Qualification: MBBS with MD
Experience: 2–5 years in clinical data review or medical monitoring
Strong knowledge of ICH-GCP guidelines and clinical trial activities
Proficiency in MS Office, MS Project, and PowerPoint
Understanding of medical terminology, risk-based monitoring methodologies, and clinical trial data systems
Excellent written and spoken English communication skills
Strong analytical, stakeholder management, and independent problem-solving capabilities
The Centralized Monitoring Unit (CMU) in Bengaluru is an integral part of Novo Nordisk’s clinical drug development operations. CMU combines medical expertise and technical analytics to ensure patient safety, protocol compliance, and high-quality clinical trial data. Our team collaborates closely with international medical specialists, statisticians, and operational programmers to detect outliers, optimize monitoring processes, and support trial teams with actionable insights.
At Novo Nordisk, we tackle serious chronic diseases with innovation, determination, and curiosity. Our inclusive culture emphasizes mutual respect, teamwork, and creative problem-solving. We empower our employees to push the boundaries of science, improve healthcare accessibility, and make a lasting impact on millions of lives globally.
Novo Nordisk is committed to diversity, equity, and inclusion in recruitment. We do not charge prospective employees fees or request personal payments during the recruitment process. Beware of fraudulent job offers impersonating Novo Nordisk representatives.
Note: Job titles may be subject to global standardization; details will be provided during the recruitment process.
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