Associate Medical Reviewer – Clinical Development
Location: Bangalore, Karnataka, India
Category: Clinical Development
Department: Central Monitoring Unit (CMU), Novo Nordisk Global Business Services (GBS)
Application Deadline: January 15, 2026
About Novo Nordisk
Novo Nordisk is a global healthcare leader committed to defeating serious chronic diseases and improving patient outcomes through innovative clinical research and medical excellence. With over 100 years of scientific advancement, the company combines a purpose-driven approach, a culture of collaboration, and an unordinary mindset to deliver life-changing therapies worldwide.
About the Department
The Central Monitoring Unit (CMU) in Bangalore operates within Clinical Drug Development, providing centralized medical monitoring and clinical data quality oversight. The team comprises skilled medical reviewers, functional programmers, and statistical monitors collaborating with Medical Specialists in Denmark. Together, they ensure patient safety, protocol compliance, and high-quality clinical trial data by identifying clinically significant outliers, performing data cleaning, and supporting risk-based monitoring methodologies.
Position Overview
Novo Nordisk is seeking a dedicated Associate Medical Reviewer to support clinical trial operations and patient safety initiatives. This role ensures high-quality, consistent medical data in line with protocols, Good Clinical Practice (GCP), ICH Guidelines, local regulations, and internal SOPs.
The Associate Medical Reviewer plays a critical role in medical data validation, risk identification, and cross-functional collaboration with trial teams to maintain inspection-ready clinical trial documentation.
Key Responsibilities
Conduct medical review of trial subjects in assigned clinical trials, ensuring protocol compliance and patient safety.
Identify and resolve medical discrepancies or data inconsistencies in collaboration with investigational site staff and healthcare professionals.
Present findings from medical reviews to relevant Medical Specialists to inform clinical decision-making.
Perform medical monitoring tasks, including protocol adherence checks, detection of clinically significant outliers, and data validation.
Document all medical review activities to ensure regulatory inspection readiness.
Collaborate with cross-functional teams, including Data Managers, Trial Managers, and Medical Specialists, to ensure high-quality deliverables.
Stay updated on therapeutic knowledge, protocol-specific guidelines, and current medical developments.
Support the development and improvement of risk-based monitoring processes and trial data management.
Qualifications
Graduate degree in MBBS + MD with 1–2 years of clinical practice or academic experience.
Strong knowledge of ICH GCP guidelines and clinical trial regulations.
Proficient in MS Office, MS Project, and PowerPoint.
Excellent understanding of medical terminology and clinical trial processes.
Experience with risk-based monitoring methodologies and clinical trial data systems.
Excellent written and spoken English with strong analytical, planning, and stakeholder management skills.
Ability to work independently, handle complex tasks, and meet project timelines.
Experience Requirements
1–2 years of relevant clinical practice or academic experience in medicine.
Familiarity with clinical trial operations, medical monitoring, and centralized monitoring workflows.
Prior experience in risk-based monitoring and clinical data validation is an advantage.
Working at Novo Nordisk
Novo Nordisk fosters a collaborative, innovative, and purpose-driven environment where employees are empowered to drive meaningful improvements in patient care. The company values curiosity, unordinary thinking, and scientific excellence to push the boundaries of medicine and healthcare accessibility globally.
Application Process
Interested candidates should submit their CV and motivational letter online via the official application portal.
Important Notice
Novo Nordisk does not extend unsolicited employment offers and does not charge fees during recruitment. Applicants should remain vigilant against fraudulent job offers.
Equal Opportunity Statement
Novo Nordisk is committed to an inclusive recruitment process and equality of opportunity for all applicants. Employment decisions are made without discrimination and in accordance with applicable laws.
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