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Associate Medical Reviewer

Novo Nordisk
1-2 years
Not Disclosed
Bangalore, India
1 May 20, 2026
Job Description
Job Type: Full Time Education: MBBS/MD Skills: Data Analysis, Document Management, Life Science, Regulatory Compliance, Waterfall Model, Environment, Experiments Design, Health And Safety (Ehs), Laboratory Equipment, Manufacturing Process, Materials Science, Process Simulation, Sop (Standard Operating Procedure), Technical Writing, Wat, GCP guidelines, gmp knowledge, HSE Knowledge , Logistics and Transportation Management, Master Data, Operational Excellence, Sap Erp, supply chain management, Supply Planning, Warehouse Management, ICD-10 CM Codes, CPT-Codes, HCPCS Codes

Associate Medical Reviewer

Company: Novo Nordisk Global Business Services (GBS)
Department: Central Monitoring Unit (CMU), Clinical Development
Category: Clinical Development
Location: Bangalore, Karnataka, India
Work Location: Novo Nordisk Global Business Services (GBS), Bengaluru


Job Overview

Novo Nordisk is seeking a dedicated Associate Medical Reviewer to join the Central Monitoring Unit (CMU) in Bangalore. This role offers an excellent opportunity for medical professionals passionate about patient safety, clinical research quality, and medical monitoring.

The selected candidate will be responsible for reviewing clinical trial subject data, identifying medical concerns, ensuring regulatory compliance, and supporting high-quality clinical trial execution through effective collaboration with cross-functional global teams.

This role is ideal for candidates with strong clinical knowledge, medical monitoring expertise, and an interest in clinical development and patient safety.


Key Responsibilities

As an Associate Medical Reviewer, you will:

  • Conduct comprehensive medical review of clinical trial subjects across assigned studies to ensure data quality, consistency, and patient safety.
  • Review clinical trial data for protocol adherence, medical consistency, and regulatory compliance.
  • Ensure compliance with:
    • Good Clinical Practice (GCP)
    • ICH Guidelines
    • Local regulatory requirements
    • Internal Standard Operating Procedures (SOPs)
  • Identify, investigate, and resolve medically significant issues, discrepancies, and data inconsistencies in collaboration with:
    • Investigational site staff
    • Healthcare professionals
    • Clinical trial teams
  • Perform core medical monitoring activities, including:
    • Protocol compliance review
    • Identification of clinically significant outliers
    • Medical data review and cleaning
    • Patient safety signal review
    • Clinical consistency checks
  • Present medical review findings and recommendations to Medical Specialists to support informed clinical decisions.
  • Maintain detailed documentation of all review activities to ensure continuous inspection and audit readiness.
  • Stay updated on:
    • Therapeutic area knowledge
    • Clinical trial protocols
    • Medical developments
    • Industry regulations and guidelines
  • Collaborate closely with:
    • Data Managers
    • Trial Managers
    • Medical Specialists
    • Clinical operations teams
  • Support delivery of high-quality clinical trial outcomes through effective centralized monitoring.

Required Qualifications

Education

Candidates must possess:

  • MBBS + MD (Mandatory)

Experience

  • 1–2 years of experience in:
    • Clinical practice
    • Medical academics
    • Clinical research (preferred)