Medical Reviewer

Job Title:  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 the integrity of clinical trial data? Do you have experience in medical review and a strong understanding of clinical trial activities? If yes, we invite you to join our Centralized Monitoring Unit (CMU) team in Bangalore as a Senior Medical Reviewer. Read on and apply today!

Position

Please note: This position involves providing medical oversight in clinical drug development. It is not a Pharmacovigilance role

The Key Responsibilities in this position will be to perform Medical Review of all trial subjects of all assigned clinical trials to ensure high quality consistent medical data. Medical Review is performed for all trial subjects to ensure patient safety and adherence to protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and Standard Operating Procedure (SOPs). Medical Reviewer ensures high quality medical data through medical review of clinical trial data. Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s) and Medical Specialists during trial conduct. Report status of medical review to project as appropriate, following the project communication plan and blinding plan. Consult with Trial Managers and Medical Specialists as appropriate to ensure medical review issues are escalated in a timely manner.

• Responsible for contribution to or participation in trial planning activities related to medical review.
• Responsible for clarifying and if possible, resolving issues of medical concern and inconsistencies in clinical trial data with staff at investigational sites.
• Responsible for presenting findings of Medical Review to relevant Medical Specialist to enable decision making. Responsible for documenting medical review in the sponsor TMF.
• Ensure close collaboration with relevant study group members, especially the Data Manager, Trial Manager(s) and Medical Specialist during trial conduct.
• Review and provide inputs to MMP as well as Medical Monitoring, Displays or other data listing required to perform medical review. The input should ensure unambiguous monitoring requirements as well as medical monitoring displays and data listing to enable efficient medical review.

Qualifications

We are looking for a highly skilled and motivated individual who meets the following criteria:

• A graduate degree in MBBS+MD with 2 to 5 years of experience
•  Good knowledge of ICH GCP guidelines.
• Demonstrated computer skills (MS Office, MS Project, PowerPoint).
• Excellent understanding of medical terminology and clinical trial activities, Experience with risk-based monitoring methodologies. - Familiarity with clinical trial data systems and tools.
• 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 Centralised Monitoring Unit (CMU) in Bengaluru is a key part of the Clinical Drug Development area at Novo Nordisk. Our department is a perfect blend of skilled medical professionals and technical programmers. Medical reviewers collaborate closely with medical specialists from Denmark to ensure the safety and well-being of clinical trial participants. Our focus is on risk-based medical monitoring, ensuring protocol compliance, identifying clinically significant outliers, and performing medical data cleaning. Functional programmers develop operational visualisations to support trial teams, while statistical monitors detect unusual data patterns, systematic errors, and potential non-compliance across trials. Join our dynamic and collaborative team to make a meaningful impact on patient safety and clinical trial excellence.

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 one hundred 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, purchasing of equipment, or funds to further the recruitment process or offer paid trainings. Be advised that Novo Nordisk does not extend unsolicited employment offers. Furthermore, Novo Nordisk does not charge prospective employees with fees or make requests for funding as a part of the recruitment process.

"Novo Nordisk is currently in the process of adjusting job titles globally. Please note that the job title listed in this advertisement may be subject to change. More detailed information will be provided during the recruitment process.”

We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. 

We’re not your typical healthcare company. In a modern world of quick fixes, we focus on solutions to defeat serious chronic diseases and promote long-term health. Our unordinary mindset is at the heart of everything we do. We seek out new ideas and put people first as we push the boundaries of science, make healthcare more accessible, and treat, prevent, and even cure diseases that affect millions of lives. Because it takes an unordinary approach to drive real, lasting change in health.