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Medical Reviewer

Novo Nordisk
Novo Nordisk
2-5 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

Medical Reviewer – Clinical Development

Category: Clinical Development
Department: Central Monitoring Unit (CMU), Global Business Services
Location: Bengaluru, Karnataka, India
Employment Type: Full-Time
Experience Required: 2–5 Years
Application Deadline: 15 January 2026


Job Overview

Novo Nordisk Global Business Services (GBS), India, is seeking a qualified and motivated 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 involves providing medical oversight in clinical drug development and is not a Pharmacovigilance role. The successful candidate will contribute to high-quality, consistent medical data through in-depth medical review of clinical trial subjects and close collaboration with cross-functional study teams.


Key Responsibilities

  • Perform comprehensive medical review of clinical trial data for all assigned study subjects to ensure patient safety and protocol adherence

  • Ensure compliance with Good Clinical Practice (GCP), ICH guidelines, local regulations, and internal SOPs

  • Collaborate closely with Data Managers, Trial Managers, Medical Specialists, and other study stakeholders during trial conduct

  • Identify, clarify, and resolve medical inconsistencies and safety-related issues in clinical trial data in collaboration with investigational sites

  • Escalate critical medical review findings in a timely manner in line with project communication and blinding plans

  • Contribute to trial planning activities related to medical review and centralized monitoring

  • Present medical review findings to relevant Medical Specialists to support informed clinical decision-making

  • Document all medical review activities accurately within the sponsor Trial Master File (TMF)

  • Review and provide inputs to Medical Monitoring Plans (MMPs), medical monitoring displays, and data listings to enable efficient and risk-based medical review

  • Support continuous improvement of centralized medical monitoring processes


Education & Experience Requirements

  • MBBS with MD qualification

  • 2 to 5 years of relevant experience in medical review, clinical development, or clinical trial oversight

  • Prior experience in centralized or risk-based medical monitoring is preferred


Required Skills & Competencies

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

  • Excellent understanding of medical terminology and clinical trial activities

  • Familiarity with risk-based monitoring methodologies

  • Experience working with clinical trial data systems and medical review tools

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

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

  • Excellent written and verbal communication skills in English

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


About the Department

The Centralized Monitoring Unit (CMU) in Bengaluru is a core component of Novo Nordisk’s Clinical Drug Development organization. The team combines medical expertise, statistical monitoring, and technical programming to deliver high-quality, risk-based medical monitoring across global clinical trials. Medical Reviewers work closely with international medical specialists to ensure protocol compliance, detect clinically relevant outliers, and support patient safety through data-driven insights.


Working at Novo Nordisk

Novo Nordisk is a global healthcare leader focused on defeating serious chronic diseases and improving long-term patient outcomes. With over a century of scientific excellence, the organization fosters a culture built on collaboration, curiosity, inclusion, and purpose-driven innovation. Employees are encouraged to challenge conventions, think boldly, and contribute to meaningful advancements in healthcare.


Equal Opportunity & Disclaimer

Novo Nordisk is committed to an inclusive recruitment process and equal opportunity for all applicants. The company does not charge any fees or request funds during recruitment and does not extend unsolicited job offers.

Please note that job titles may be subject to global alignment and could change during the recruitment process.


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