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Associate Medical Reviewer

Novo Nordisk
Novo Nordisk
1-2 years
preferred by company
10 Jan. 14, 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

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


Job Overview

Novo Nordisk Global Business Services (GBS), India, is seeking a highly motivated Associate Medical Reviewer to join its Central Monitoring Unit (CMU) in Bengaluru. This role is integral to ensuring patient safety, data integrity, and medical quality across global clinical trials.

The position offers an excellent opportunity for qualified medical professionals to contribute to medical monitoring, centralized review, and clinical data quality, while collaborating with international stakeholders and medical specialists.


Key Responsibilities

As an Associate Medical Reviewer, you will be responsible for:

  • Conducting comprehensive medical reviews of clinical trial subjects to ensure accuracy, consistency, and high-quality medical data

  • Ensuring patient safety and compliance with study protocols, ICH-GCP guidelines, SOPs, and local regulatory requirements

  • Identifying, assessing, and resolving medical issues, inconsistencies, and clinically significant outliers in trial data

  • Collaborating with investigational site staff, healthcare professionals, and internal trial teams to address medical concerns

  • Presenting medical review findings to Medical Specialists to support informed clinical decisions

  • Performing medical monitoring activities, including protocol compliance checks and data consistency assessments

  • Maintaining complete and accurate documentation to ensure inspection and audit readiness

  • Staying updated with therapeutic knowledge, protocol-specific requirements, and current medical advancements

  • Working closely with Data Managers, Trial Managers, Statistical Monitors, and Medical Specialists to deliver high-quality outcomes


Required Qualifications & Experience

Mandatory Requirements:

  • MBBS with MD (postgraduate medical qualification)

  • 1–2 years of experience in clinical practice, academics, or clinical research

  • Strong working knowledge of ICH-GCP guidelines and clinical trial regulations

  • Excellent understanding of medical terminology and clinical trial processes

Preferred Skills & Competencies:

  • Experience or familiarity with risk-based monitoring methodologies

  • Knowledge of clinical trial data systems and medical review tools

  • Proficiency in MS Office (Word, Excel, PowerPoint) and MS Project

  • Excellent written and verbal communication skills in English

  • Strong analytical, problem-solving, and result-oriented mindset

  • Ability to manage complex tasks independently with effective stakeholder management skills


About the Department – Central Monitoring Unit (CMU)

The Centralized Monitoring Unit (CMU) in Bengaluru is part of Novo Nordisk’s Clinical Drug Development function. The department comprises a multidisciplinary team of Medical Reviewers, Functional Programmers, and Statistical Monitors.

Medical Reviewers collaborate closely with Medical Specialists based in Denmark to ensure patient safety and protocol compliance. The team leverages centralized and risk-based monitoring approaches to identify data trends, clinically relevant outliers, and potential compliance risks, contributing significantly to the quality and success of global clinical trials.


Working at Novo Nordisk

For more than 100 years, Novo Nordisk has focused on defeating serious chronic diseases through science, innovation, and an unordinary mindset. The company is driven by a strong purpose, mutual respect, and a commitment to improving patient lives worldwide.

Novo Nordisk fosters a culture that values curiosity, collaboration, and continuous learning, offering employees opportunities to grow while making a meaningful impact on global healthcare.


Important Notice

Novo Nordisk does not charge any fees or request payments during the recruitment process. Applicants are advised to remain cautious of fraudulent job offers claiming association with Novo Nordisk or its affiliates.

Please note that Novo Nordisk is currently aligning job titles globally; therefore, the title mentioned in this posting may be subject to change during the recruitment process.


Diversity & Inclusion

Novo Nordisk is committed to an inclusive recruitment process and provides equal employment opportunities to all applicants, regardless of background.