Associate Medical Reviewer – Clinical Development
Company: Novo Nordisk
Department: Central Monitoring Unit (CMU), Global Business Services (GBS)
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Application Deadline: 15 January 2026
Industry: Clinical Research & Drug Development
Job Overview
Novo Nordisk Global Business Services (GBS) India is seeking a qualified Associate Medical Reviewer to join its Central Monitoring Unit in Bengaluru. This role is central to ensuring patient safety, protocol compliance, and high-quality clinical trial data across global studies.
The Associate Medical Reviewer will perform medical monitoring and centralized review activities in accordance with ICH-GCP guidelines, global regulatory requirements, and internal SOPs. This position offers exposure to international clinical trial operations and collaboration with global medical and statistical teams.
Experience Required
1–2 years of experience in clinical practice or academic medical settings
Prior exposure to clinical trials, medical data review, or risk-based monitoring is preferred
Experience in regulated environments adhering to ICH-GCP standards is advantageous
Educational Qualification
MBBS + MD (Mandatory)
Key Responsibilities
Conduct comprehensive medical review of clinical trial subjects to ensure data integrity, consistency, and patient safety.
Perform centralized medical monitoring, including protocol compliance checks and identification of clinically significant outliers.
Detect and resolve inconsistencies or medical concerns in collaboration with investigational sites and healthcare professionals.
Present medical review findings to Medical Specialists to support informed decision-making.
Ensure documentation of medical review activities to maintain continuous inspection readiness.
Collaborate with Data Managers, Trial Managers, Statistical Monitors, and Functional Programmers for high-quality deliverables.
Stay updated on therapeutic areas, clinical protocols, and evolving regulatory guidelines.
Contribute to medical data cleaning and risk-based monitoring strategies.
Required Skills & Competencies
Strong knowledge of ICH-GCP guidelines and clinical research regulations
Excellent understanding of medical terminology and clinical trial processes
Familiarity with risk-based monitoring methodologies
Experience with clinical trial data systems and review tools
Proficiency in MS Office (Excel, PowerPoint, MS Project)
Strong analytical and result-oriented approach
Excellent written and verbal communication skills
Ability to manage complex tasks independently
Effective stakeholder management and cross-functional collaboration
About the Central Monitoring Unit (CMU)
The CMU in Bengaluru is part of Novo Nordisk’s Clinical Drug Development division. The unit integrates Medical Reviewers, Functional Programmers, and Statistical Monitors to deliver proactive centralized monitoring solutions.
Medical Reviewers work closely with Medical Specialists based in Denmark to ensure patient safety, protocol adherence, and accurate clinical data evaluation. Statistical and technical teams support with advanced data visualization and detection of unusual data patterns to strengthen trial oversight and compliance.
Why Join Novo Nordisk?
With over a century of innovation in chronic disease management, Novo Nordisk is a global healthcare leader committed to improving patient lives through science-driven solutions. Employees benefit from a collaborative international environment, strong compliance culture, and structured career growth in clinical research and drug development.
Important Notice
Novo Nordisk does not charge any fees during the recruitment process and does not extend unsolicited employment offers. Applicants are advised to verify all communication channels before sharing personal information.
SEO Keywords:
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