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Associate Medical Reviewer

Novo Nordisk
Novo Nordisk
1-2 years
Not Disclosed
10 Dec. 29, 2025
Job Description
Job Type: Full Time Education: B.Sc/M.Sc/M.Pharma/B.Pharma/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 / Medical Monitoring
Department: Centralized Monitoring Unit (CMU), Global Business Services
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Experience Required: 1–2 Years
Application Deadline: 15 January 2026
Organization: Novo Nordisk Global Business Services (GBS), India


About the Role

Novo Nordisk is seeking a highly motivated Associate Medical Reviewer to join its Centralized Monitoring Unit (CMU) in Bengaluru. This role plays a critical part in ensuring patient safety, data integrity, and regulatory compliance across global clinical trials.

The position is ideal for medical professionals looking to transition into clinical research, medical monitoring, and centralized trial oversight within a globally respected pharmaceutical organization.


Key Responsibilities

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

  • Conducting comprehensive medical reviews of clinical trial subjects across assigned studies

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

  • Identifying medical inconsistencies, safety signals, and clinically significant data outliers

  • Collaborating with investigational site staff, healthcare professionals, and internal trial teams to resolve medical queries

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

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

  • Maintaining thorough documentation of all review activities to ensure inspection and audit readiness

  • Staying updated on therapeutic areas, protocol-specific requirements, and evolving medical standards

  • Working closely with Data Managers, Trial Managers, Medical Specialists, and centralized monitoring teams to deliver high-quality clinical outcomes


Required Qualifications and Skills

Mandatory Requirements:

  • MBBS with MD qualification

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

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

  • Excellent understanding of medical terminology and clinical trial processes

  • Proficiency in MS Office tools (Word, Excel, PowerPoint); familiarity with clinical trial systems is an advantage

  • Experience or exposure to risk-based monitoring methodologies

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

  • Excellent written and spoken English communication

  • Ability to manage complex tasks independently and collaborate effectively with global stakeholders


About the Department

The Centralized Monitoring Unit (CMU) in Bengaluru is part of Novo Nordisk’s Clinical Drug Development organization. The department combines medical expertise and advanced analytics to ensure proactive oversight of global clinical trials.

Medical Reviewers work closely with Medical Specialists based in Denmark, focusing on patient safety, protocol adherence, and medical data quality. The team also includes Functional Programmers and Statistical Monitors who develop advanced visualizations and detect unusual data patterns, systematic errors, and compliance risks. This collaborative environment enables high-quality, data-driven clinical trial monitoring.


Working at Novo Nordisk

Novo Nordisk is a global healthcare leader with a century-long legacy of innovation in treating serious chronic diseases. The company is driven by an unordinary mindset—one that values scientific excellence, curiosity, collaboration, and respect for people.

Employees at Novo Nordisk contribute to meaningful work that impacts millions of lives worldwide, while being part of a culture that promotes inclusion, continuous learning, and long-term career growth.


Equal Opportunity and Inclusion

Novo Nordisk is committed to providing equal employment opportunities to all applicants. Recruitment decisions are based solely on qualifications, experience, and business needs, ensuring a fair and inclusive hiring process.


Important Notice

Novo Nordisk does not extend unsolicited job offers and does not charge candidates any fees during the recruitment process. Applicants are advised to remain vigilant against fraudulent job communications claiming association with Novo Nordisk or its affiliates.

Please note that Novo Nordisk is currently aligning job titles globally; the advertised title may be subject to change during the recruitment process.