Novo Nordisk Global Business Services (GBS), India is recruiting an Associate Medical Reviewer in the Central Monitoring Unit at Bengaluru. This role in clinical development and medical monitoring offers a chance to ensure patient safety, high-quality clinical trial data, and protocol compliance in global trials.
Ideal for MBBS + MD graduates with 1–2 years of clinical practice or academic experience passionate about contributing to treatments for serious chronic diseases.
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About the Company
Novo Nordisk is a leading global healthcare company with over 100 years of innovation, specializing in defeating serious chronic diseases such as diabetes, obesity, and rare endocrine disorders. Headquartered in Denmark, the company drives groundbreaking research, develops life-changing therapies, and focuses on long-term health solutions rather than quick fixes.
The Central Monitoring Unit (CMU) in Bangalore, part of Clinical Drug Development, combines medical expertise (Medical Reviewers) with technical skills (Functional Programmers and Statistical Monitors).
The team collaborates closely with Medical Specialists in Denmark to perform centralized, risk-based monitoring, ensuring patient well-being, data integrity, and regulatory compliance across global clinical trials.
Job Details
- Company Name: Novo Nordisk Global Business Services (GBS), India
- Position: Associate Medical Reviewer
- Department: Central Monitoring Unit, Clinical Drug Development
- Experience Required: 1–2 years in clinical practice or academics
- Qualification: MBBS + MD
- Location: Bengaluru (Bangalore), Karnataka, India
- Work Type: On-site / Hybrid (as per Novo Nordisk GBS norms)
Job Description
As an Associate Medical Reviewer in the CMU, you will play a critical role in centralized medical monitoring of assigned clinical trials. The position focuses on reviewing medical data for consistency, identifying safety concerns, ensuring protocol adherence, and supporting high-quality trial outcomes.
Key Responsibilities
- Conduct thorough medical review of all trial subjects to ensure high-quality, consistent medical data
- Safeguard patient safety and verify adherence to protocols, GCP, ICH Guidelines, local regulations, and SOPs
- Identify and resolve medical concerns or data inconsistencies by collaborating with investigational site staff and healthcare professionals
- Present medical review findings to Medical Specialists for informed decision-making
- Perform medical monitoring tasks: protocol compliance checks, detection of clinically significant outliers, and data consistency verification
- Document all review activities to maintain inspection readiness at all times
- Stay current with therapeutic knowledge, protocol guidelines, and emerging medical developments
- Collaborate with trial teams (Data Managers, Trial Managers, Medical Specialists) to deliver quality results
Skills & Qualifications Required
- MBBS + MD degree (mandatory)
- 1–2 years of experience in clinical practice or academics
- Strong knowledge of ICH GCP guidelines
- Excellent understanding of medical terminology and clinical trial processes
- Experience or familiarity with risk-based monitoring methodologies
- Proficiency in clinical trial data systems and tools
- Demonstrated computer skills (MS Office, MS Project, PowerPoint)
- Excellent written and spoken English
- Strong analytical, result-oriented, planning, and independent task-handling abilities
- Effective communication and stakeholder management skills
Benefits & Perks
- Opportunity to contribute to innovative treatments for chronic diseases
- Work in a collaborative, dynamic team blending medical and technical expertise
- Exposure to global clinical trials and centralized monitoring practices
- Inclusive culture with focus on equality, professional growth, and work-life balance
- Be part of a purpose-driven company committed to long-term health impact
How to Apply
Apply through the official Novo Nordisk careers portal: https://www.novonordisk.com/careers.html or https://careerhub.novonordisk.com
Search for “Associate Medical Reviewer” or similar roles in Bengaluru/India. Submit your updated resume and relevant documents.
Verified Post
Verification: To confirm the legitimacy of this posting, you can view the original announcement on the Novo Nordisk Career page.
For more pharma jobs in clinical research, medical affairs, and Bangalore opportunities, visit Pharma Recruiter.
Important Note: Novo Nordisk does NOT charge fees, request funds, or offer unsolicited jobs. Beware of fraudulent offers—only official channels are legitimate.
Why Join Novo Nordisk?
Novo Nordisk stands out with an “unordinary mindset,” relentless curiosity, and a deep commitment to defeating chronic diseases. Join a company that values people, pushes scientific boundaries, and delivers real, lasting change in healthcare.
Enjoy a supportive environment, global collaboration, and the chance to make a meaningful difference in patients’ lives every day.
Frequently Asked Questions (FAQs)
What is the minimum qualification for Associate Medical Reviewer at Novo Nordisk?
MBBS + MD with 1–2 years of clinical practice or academic experience.
What department and location is this role in?
Central Monitoring Unit (CMU), Clinical Drug Development, based in Bengaluru, India.
Does the role require prior clinical trial experience?
Not mandatory—focus is on medical knowledge, GCP understanding, and clinical practice/academics experience.
How can I avoid recruitment fraud from Novo Nordisk?
Apply only through official Novo Nordisk careers websites. The company never charges fees or requests money/equipment purchases.
