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Associate Medical Reviewer

1-2 years
Not Disclosed
10 July 1, 2025
Job Description
Job Type: Hybrid Education: B.Sc./M.Sc/B.Pharm/M.Pharm/Life Science 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 Trials | Bangalore

Job Summary:

Novo Nordisk is seeking an Associate Medical Reviewer to join its Centralised Monitoring Unit (CMU) in Bangalore, India. This role is pivotal to ensuring medical data quality and patient safety across clinical trials by performing in-depth medical data reviews, collaborating with trial teams, and supporting adherence to Good Clinical Practice (GCP), ICH guidelines, and regulatory standards. Ideal for medical graduates (MBBS/MD) with 1–2 years of clinical research or medical monitoring experience, this full-time position offers the opportunity to contribute to life-changing therapies in a dynamic, global setting.


Key Responsibilities:

  • Perform thorough medical reviews of clinical trial data across various therapy areas

  • Ensure patient safety and protocol compliance through risk-based medical monitoring

  • Collaborate with Data Managers, Trial Managers, and Medical Specialists during trial conduct

  • Present findings to medical teams and document medical reviews in the sponsor’s TMF

  • Contribute to trial planning and develop medical monitoring displays and data listings

  • Support clarification and resolution of medical concerns or data inconsistencies

  • Provide training on medical review processes to new team members

  • Adhere to timelines for assigned projects, supporting medical integrity and compliance


Required Skills & Qualifications:

  • MBBS or MD degree in a clinical specialty

  • 1+ years of experience in Clinical Drug Development, including medical review, monitoring, or investigator responsibilities

  • Familiarity with ICH guidelines and GCP principles

  • Understanding of clinical trial processes and medical terminology

  • Strong English communication skills (written and spoken)

  • Proficiency in MS Office, PowerPoint, and MS Project

  • Project management experience (1–2 years preferred)

  • Analytical, results-oriented, and team-collaborative mindset


Perks & Benefits:

  • Work with a global healthcare leader impacting millions of lives

  • Inclusive and collaborative work environment

  • Professional growth and training opportunities

  • Contribute to life-changing clinical development initiatives

  • Join a company recognized among the world’s most valuable healthcare employers


Company Description:

Novo Nordisk, a global leader in chronic disease care and clinical drug development, is known for innovation in diabetes, obesity, and other serious conditions. With 100 years of healthcare excellence and over 72,000 employees worldwide, Novo Nordisk is committed to building a healthier world through diversity, inclusion, and collaboration.


Work Mode:

On-site – Based in Bangalore, India


Call-to-Action:

Ready to contribute to global patient safety and clinical trial excellence? Apply now to join Novo Nordisk’s medical review team in Bangalore. Applications are open until 7th July 2025.