Medical Reviewer Jobs at Novo Nordisk – Apply Now
Medical Reviewer Jobs: Novo Nordisk Global Business Services (GBS), Bengaluru, is hiring experienced medical professionals for the role of Medical Reviewer within its Centralized Monitoring Unit (CMU). This role is ideal for doctors who want to work at the intersection of clinical medicine, data integrity, and patient safety in global drug development—without being a pharmacovigilance role. The position offers an opportunity to contribute directly to high-quality clinical trial outcomes in a globally respected organization.
Medical Reviewer Jobs – Details
- Job Title: Medical Reviewer
- Department: Central Monitoring Unit (CMU), Clinical Development
- Location: Bengaluru, Karnataka, India
- Employment Type: Full-time
About the Company
Novo Nordisk is a global healthcare company with over a century of innovation in defeating serious chronic diseases such as diabetes, obesity, and rare disorders. With operations across the world, Novo Nordisk is known for its strong ethical foundation, patient-first mindset, and commitment to scientific excellence.
The Global Business Services (GBS) unit in India plays a critical role in supporting Novo Nordisk’s global clinical development operations by delivering high-quality medical, technical, and analytical expertise.
Medical Reviewer Jobs – Qualifications
- MBBS + MD from a recognized medical institution
- 2 to 5 years of relevant experience in clinical trials or clinical drug development
- Strong knowledge of ICH-GCP guidelines
- Excellent understanding of clinical trial activities and medical terminology
- Familiarity with clinical trial data systems and risk-based monitoring methodologies
- Strong analytical, documentation, and problem-solving skills
- Excellent written and spoken English
- Ability to manage complex tasks independently and collaborate across global teams
About the Role
The medical reviewer provides medical oversight in clinical drug development by reviewing clinical trial data to ensure patient safety, protocol compliance, and data integrity. This is a non-pharmacovigilance role focused on centralized medical monitoring and collaboration with global trial teams.
The role requires close interaction with data managers, trial managers, and medical specialists to identify clinically relevant findings and support informed decision-making during trial conduct.
Key Responsibilities
- Perform a comprehensive medical review of clinical trial data for all assigned trial subjects
- Ensure adherence to study protocols, ICH-GCP guidelines, SOPs, and local regulatory requirements
- Identify medical inconsistencies, safety concerns, and clinically significant outliers in trial data
- Collaborate closely with Data Managers, Trial Managers, and Medical Specialists throughout trial conduct
- Clarify and resolve medical data issues with investigational site staff
- Present medical review findings to Medical Specialists for decision-making
- Contribute to trial planning activities related to medical review
- Review and provide medical input to Medical Monitoring Plans (MMP), data listings, and monitoring displays
- Ensure proper documentation of medical review activities in the sponsor Trial Master File (TMF)
- Report medical review status as per project communication and blinding plans
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