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Associate Medical Reviewer

Novo Nordisk
Novo Nordisk
1-2 years
preferred by company
10 Jan. 8, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Medical Reviewer – Clinical Development

Location: Bangalore, Karnataka, India
Department: Central Monitoring Unit (CMU), GBS Bengaluru
Category: Clinical Development
Company: Novo Nordisk Global Business Services (GBS), India
Application Deadline: 15 January 2026


Job Overview

Novo Nordisk is seeking a highly motivated Associate Medical Reviewer to join our Centralized Monitoring Unit (CMU) in Bangalore. This role is ideal for early-career medical professionals who are passionate about patient safety, clinical trial quality, and medical monitoring. The Associate Medical Reviewer will play a pivotal role in ensuring consistent, high-quality clinical trial data while contributing to the integrity of global drug development initiatives.

As part of a multidisciplinary team, you will collaborate with Medical Specialists, Data Managers, Trial Managers, and technical experts to drive centralized monitoring and maintain adherence to regulatory standards.


Key Responsibilities

  • Conduct medical review of all trial subjects in assigned clinical trials to ensure data quality, protocol compliance, and patient safety.

  • Monitor adherence to ICH-GCP guidelines, SOPs, and local regulations.

  • Identify, document, and resolve issues of medical concern or inconsistencies in trial data in collaboration with site staff and healthcare professionals.

  • Present findings from medical reviews to relevant Medical Specialists for informed decision-making.

  • Perform medical monitoring tasks, including protocol compliance checks, risk-based monitoring, identifying clinically significant outliers, and maintaining data integrity.

  • Maintain meticulous documentation of all medical review activities to ensure inspection readiness.

  • Stay updated on therapeutic knowledge, protocol-specific guidelines, and emerging developments in clinical research.

  • Collaborate closely with trial teams to ensure timely, high-quality deliverables.


Required Qualifications

  • Medical degree: MBBS + MD

  • Experience: 1–2 years in clinical practice, medical academics, or clinical research

  • Strong knowledge of ICH-GCP guidelines and clinical trial methodology

  • Proficiency with MS Office, MS Project, PowerPoint

  • Understanding of medical terminology and risk-based monitoring approaches

  • Familiarity with clinical trial data systems and tools

  • Excellent written and spoken English communication skills

  • Strong analytical skills, attention to detail, and ability to independently manage tasks

  • Effective stakeholder management and collaborative mindset


About the Department

The Centralized Monitoring Unit (CMU) in Bangalore is an integral part of Novo Nordisk’s Clinical Drug Development organization. Our team blends medical expertise with technical and statistical monitoring to ensure high-quality clinical trial outcomes.

  • Medical Reviewers collaborate with Medical Specialists globally to monitor patient safety, protocol compliance, and data integrity.

  • Functional Programmers develop visualizations and dashboards to support centralized monitoring.

  • Statistical Monitors detect unusual data patterns, potential compliance issues, and systematic errors.

This collaborative environment provides a unique opportunity to contribute to global clinical trial excellence while building a strong foundation in medical monitoring and clinical development.


Why Novo Nordisk

Novo Nordisk is a global leader in healthcare, committed to defeating serious chronic diseases and improving long-term patient outcomes. We foster a culture of curiosity, collaboration, and innovation, empowering employees to make meaningful contributions that impact patients worldwide.

Benefits & Opportunities:

  • Work in a fast-growing, innovative, and collaborative environment

  • Exposure to global clinical trial practices and medical monitoring techniques

  • Opportunities for professional development and career growth

  • Inclusive and diverse workplace culture


Application Instructions

Interested candidates should apply online by uploading their updated CV. Internal candidates should inform their line managers before applying.

Important Notice: Novo Nordisk does not charge fees or solicit funds during recruitment. Beware of fraudulent offers impersonating the company.

Novo Nordisk is committed to equal opportunity and inclusive hiring practices.


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