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Medical Reviewer

1-2 years
Not Disclosed
10 July 1, 2025
Job Description
Job Type: Hybrid Education: MBBS or MD 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 Trials | Novo Nordisk, Bangalore

Job Summary:

Novo Nordisk is hiring a Medical Reviewer in Bangalore to support its Centralised Monitoring Unit (CMU) in ensuring clinical trial data quality and patient safety across a global portfolio. The role focuses on reviewing clinical data for protocol compliance, identifying potential safety issues, and collaborating closely with study teams. If you're a medical graduate (MBBS/MD) with 3+ years of clinical development experience, this is your opportunity to advance your career in a leading healthcare organization making a global impact.


Key Responsibilities:

  • Conduct medical review of clinical trial data across therapy areas to ensure consistency and safety

  • Participate in planning, monitoring, and documentation of clinical data review processes

  • Identify and resolve clinical data discrepancies and medical concerns with site staff

  • Present findings to medical teams to support clinical decision-making

  • Collaborate with Data Managers, Trial Managers, and Medical Specialists

  • Contribute to the development of Medical Monitoring Plans and review data listings

  • Train new team members on medical review processes and trial data quality

  • Maintain compliance with ICH-GCP, SOPs, and local regulatory standards


Required Skills & Qualifications:

  • MBBS or MD in a clinical specialty

  • 3+ years of experience in Clinical Drug Development (e.g., Medical Data Review, Medical Monitoring, Investigator, Safety Surveillance)

  • 1–2 years of project management experience preferred

  • Strong understanding of ICH and GCP guidelines

  • Proficiency in MS Office, MS Project, and PowerPoint

  • Strong analytical and documentation skills

  • Excellent command of English (spoken and written)

  • Familiarity with clinical trial design, medical terminology, and data analysis


Perks & Benefits:

  • Be part of a top 20 global healthcare company

  • Work on international clinical research projects

  • Inclusive and diverse work culture

  • Professional development and training opportunities

  • Competitive compensation (based on experience)

  • Opportunity to impact global healthcare and patient lives


Company Description:

Novo Nordisk is a global leader in diabetes and chronic disease care, delivering innovative clinical solutions for over a century. With 72,000+ employees globally, Novo Nordisk drives cutting-edge research in clinical drug development and prioritizes sustainability, inclusion, and life-changing healthcare outcomes.


Work Mode:

On-site – Bangalore, India


Call-to-Action:

Are you ready to shape the future of global clinical research? Apply now to join Novo Nordisk as a Medical Reviewer. Submit your application before 7th July 2025 and become part of a life-changing mission.