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Novo Nordisk

Senior Medical Reviewer

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Job Description

Job description

Job Title: Senior 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!

The Position

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

As a Senior Medical Reviewer, you will play a critical role in ensuring the quality and consistency of medical data across clinical trials. Your key responsibilities will include:

  • Conducting medical reviews of clinical trial data to ensure patient safety, protocol compliance, and adherence to regulatory requirements. Collaborating closely with study group members, including Data Managers, Trial Managers, and Medical Specialists, to ensure high-quality deliverables.

  • Identifying and resolving issues of medical concern and inconsistencies in clinical trial data with investigational site staff and healthcare professionals. Presenting findings of medical reviews to relevant Medical Specialists to enable informed decision-making.

  • Documenting medical reviews in the sponsor Trial Master File (TMF) and always ensuring inspection readiness. Performing quality control of medical review tasks and findings.

  • Providing training and mentoring to new team members, including therapeutic area training and process guidance. Contributing to shared best practices, process improvements, and other activities to ensure the team meets timelines and quality standards.

  • Planning and managing resources for medical review tasks, including timeline planning and resource allocation.

Qualifications

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

  • A graduate degree in MBBS+MD with 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.

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About Company

Novo Nordisk A/S is a Danish multinational pharmaceutical company headquartered in Bagsv&#230&#x3B;rd, Denmark, with production facilities in eight countries, and affiliates or offices in 5 countries. Novo Nordisk is controlled by majority shareholder Novo Holdings A/S which holds approximately 25% of its shares and a supermajority (45%) of its voting shares.

Job ID: 136995259