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Senior Medical Reviewer

3+ years
Not Disclosed
10 July 1, 2025
Job Description
Job Type: Full Time 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

 

Senior Medical Reviewer – Clinical Drug Development | Novo Nordisk, Bangalore

Job Summary:

Novo Nordisk is seeking a Senior Medical Reviewer to lead clinical trial data review within its Centralised Monitoring Unit (CMU) in Bangalore. This pivotal role focuses on ensuring the integrity, consistency, and medical quality of clinical data, while safeguarding patient safety and adherence to Good Clinical Practice (GCP) and ICH guidelines. Ideal candidates are MBBS/MD professionals with 3+ years of experience in medical monitoring or clinical drug development. Step into a dynamic, global healthcare environment and make an impact on millions of lives.


Key Responsibilities:

  • Conduct thorough medical review of clinical trial data across multiple therapeutic areas

  • Collaborate with study teams including Data Managers, Trial Managers, and Medical Specialists

  • Identify and resolve clinical inconsistencies or potential safety issues

  • Contribute to trial planning and develop Medical Monitoring Plans (MMP)

  • Present medical findings to stakeholders to support timely decision-making

  • Train new team members on review processes and project expectations

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

  • Document reviews in Trial Master File (TMF) and support data integrity checks


Required Skills & Qualifications:

  • MBBS or MD in Medicine or related clinical specialty

  • Minimum 3 years’ experience in clinical drug development (medical review, monitoring, safety surveillance, etc.)

  • 1–2 years of project management experience preferred

  • Solid understanding of ICH guidelines and GCP principles

  • Proficient in MS Office, PowerPoint, and project management tools

  • Strong medical terminology knowledge and clinical trial process experience

  • Excellent analytical, communication, and documentation skills

  • Fluent in English (written and spoken)


Perks & Benefits:

  • Work at one of the top global healthcare companies

  • Engage in high-impact clinical development projects

  • Collaborative and inclusive work culture

  • Career growth with learning and leadership opportunities

  • Work-life balance with supportive team dynamics

  • Full-time, permanent role with competitive compensation (based on experience)

  • Work mode: On-site at Bangalore with global collaboration


Company Description:

Novo Nordisk is a global healthcare leader driving innovation in chronic disease treatment and clinical drug development. With over 72,000 employees worldwide and a 100-year legacy, Novo Nordisk delivers transformative solutions in diabetes care, rare diseases, and clinical research. The Bangalore GBS unit supports global clinical trials, medical monitoring, and centralized review operations.


Work Mode:

On-site – Bangalore, India


Call-to-Action:

Ready to make a difference in global clinical development? Apply now for the Senior Medical Reviewer role at Novo Nordisk before 7th July 2025 and become part of a purpose-driven team transforming lives through science.