Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Medical Reviewer

Novo Nordisk
Novo Nordisk
2-5 years
preferred by company
Bangalore, India
1 May 13, 2026
Job Description
Job Type: Education: M.Pharm/B.Pharm or M.Sc. 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, ICD-10 CM, CPT, HCPCS Coding

Job Title: Medical Reviewer

Location: Bangalore, Karnataka, India
Job Type: Full-Time
Experience Required: 2–5 Years (Freshers are not eligible)
Industry: Clinical Development / Clinical Research / Medical Monitoring / Pharmaceuticals / Healthcare
Department: Central Monitoring Unit (CMU) / Clinical Drug Development

About the Role
We are seeking a highly analytical and clinically experienced Medical Reviewer to support centralized clinical trial medical monitoring and patient safety oversight within a global clinical development environment. This role is ideal for medical professionals with expertise in clinical trial medical review, protocol compliance, clinical data evaluation, risk-based monitoring, and patient safety monitoring.

The ideal candidate will perform comprehensive medical review of clinical trial participant data to ensure data quality, patient safety, protocol adherence, and regulatory compliance throughout the clinical trial lifecycle. This is a critical clinical development role focused on medical oversight and data integrity rather than pharmacovigilance operations.

This opportunity is particularly suited for physicians interested in clinical development, centralized monitoring, and advanced medical data review.

Key Responsibilities

Clinical Trial Medical Review & Patient Safety Oversight

  • Conduct comprehensive medical review of clinical trial participant data across assigned clinical studies to ensure patient safety and medical data integrity.
  • Review subject-level clinical data to identify medical inconsistencies, protocol deviations, safety concerns, and clinically significant findings.
  • Ensure high-quality, medically consistent clinical trial data throughout study conduct.
  • Escalate medically significant observations to relevant clinical stakeholders for timely decision-making.

Protocol Compliance & Clinical Monitoring Support

  • Ensure clinical trial conduct aligns with study protocols, ICH-GCP guidelines, local regulations, sponsor SOPs, and clinical monitoring requirements.
  • Support adherence to risk-based medical monitoring frameworks and centralized monitoring processes.
  • Identify protocol compliance issues and assist with resolution in collaboration with study teams.
  • Contribute to maintenance of clinical oversight and regulatory readiness.

Clinical Data Review & Medical Data Quality Management

  • Analyze clinical trial datasets, medical listings, monitoring outputs, and data review tools to identify anomalies and trends.
  • Support medical data cleaning activities, issue clarification, and resolution of clinical inconsistencies.
  • Review medical monitoring plans, data displays, dashboards, and analytical outputs to optimize review efficiency.
  • Ensure clear documentation of review outcomes in the Trial Master File (TMF) and other required systems.

Cross-Functional Collaboration & Clinical Stakeholder Engagement

  • Collaborate closely with Trial Managers, Data Managers, Medical Specialists, clinical operations teams, and study stakeholders during trial execution.
  • Present medical review findings and support clinical decision-making discussions.
  • Work with investigational sites to clarify data discrepancies and medically relevant observations.
  • Support effective communication of medical review status according to project communication plans and blinding requirements.

Trial Planning & Medical Oversight Support

  • Contribute to clinical trial planning activities related to medical review strategies, monitoring requirements, and oversight frameworks.
  • Provide input into medical monitoring plans, data review requirements, and operational oversight processes.
  • Support optimization of centralized medical monitoring methodologies.

Required Qualifications

  • MBBS + MD (Doctor of Medicine) or equivalent advanced medical qualification.
  • 2–5 years of relevant experience in clinical research, medical review, clinical development, medical monitoring, or related pharmaceutical clinical roles.
  • Strong understanding of ICH-GCP guidelines, clinical trial conduct, patient safety oversight, and medical data review processes.
  • Experience in risk-based monitoring, centralized clinical monitoring, or medical data review is preferred.
  • Familiarity with clinical trial systems, medical data review tools, and operational monitoring platforms.
  • Excellent understanding of medical terminology, clinical research methodologies, and protocol compliance standards.
  • Strong analytical thinking, independent decision-making, documentation accuracy, and problem-solving capabilities.
  • Excellent written and spoken English communication skills.
  • Strong stakeholder collaboration and clinical communication abilities.

Preferred Skills

  • Clinical trial medical review
  • Medical monitoring
  • Centralized monitoring
  • Risk-based monitoring (RBM)
  • Clinical data review
  • Patient safety oversight
  • Protocol compliance review
  • Trial Master File (TMF) documentation
  • Medical data cleaning
  • Clinical development support
  • Cross-functional clinical collaboration
  • Clinical research analytics