Medical Reviewer – Centralised Monitoring Unit (CMU)
Company: Novo Nordisk Global Business Solutions (GBS) India
Location: Bangalore, Karnataka, India
Function: Clinical Development (Risk‑Based/Centralised Medical Monitoring)
Application Deadline: 31 July 2025
Work Mode: On-site / Hybrid (CMU, Bangalore)
Compensation / Salary: Not disclosed in the job description
Job Summary
Novo Nordisk’s Centralised Monitoring Unit (CMU) in Bangalore is looking for an experienced Medical Reviewer to perform risk‑based medical monitoring (RBM) and comprehensive medical data review across therapy areas. You’ll ensure patient safety, protocol adherence, and ICH‑GCP compliance, collaborate with global study teams (Data Managers, Trial Managers, Medical Specialists), and document medical reviews in the TMF. Note: This is not a Pharmacovigilance role.
Key Responsibilities
Lead comprehensive medical reviews of clinical trial data to ensure quality, consistency, protocol adherence, and patient safety.
Contribute to trial planning and define quality check measures for medical review.
Identify, clarify, and resolve medically significant issues and inconsistencies with investigative sites.
Present medical review findings to Medical Specialists to support decision‑making; document reviews in TMF.
Collaborate closely with Data Managers, Trial Managers, and Medical Specialists; train new team members on project/process.
Review and provide inputs to Medical Monitoring Plans (MMPs), medical monitoring displays, and data listings to enable efficient medical review.
Escalate issues proactively to protect trial integrity and regulatory compliance (ICH‑GCP, SOPs, local regulations).
Drive continuous improvement within centralized & risk‑based monitoring frameworks.
Required Skills & Qualifications
MBBS/MD (Medicine or other clinical specialties) with relevant clinical patient management or clinical research experience.
≥3 years of relevant experience in Clinical Drug Development (Medical Data Review, Medical Monitoring, Investigator, Safety Surveillance, Scientific Clinical Development, etc.).
1–2 years of project management experience (essential).
Solid understanding of ICH guidelines and Good Clinical Practice (GCP).
Strong knowledge of medical terminology, clinical trial processes, and data interpretation.
Proficient with MS Office, MS Project, PowerPoint.
Excellent analytical, communication (written & spoken English), and stakeholder management skills.
Results‑oriented with the ability to work in a dynamic, cross‑functional, global environment.
Perks & Benefits
Global exposure within a world‑class CMU combining medical reviewers, functional programmers & statistical monitors.
Career development & progression, structured training, and strong people‑centric culture (Total Self).
Opportunity to impact patient safety and data quality across global clinical trials in a top‑20 global company by market cap.
Company Description
Novo Nordisk is a global healthcare leader with a 100‑year legacy, committed to defeating serious chronic diseases. With 72,000+ employees impacting 40+ million patients daily, the company combines innovation, inclusivity, and purpose to deliver life‑changing therapies worldwide.
Work Mode
On-site / Hybrid – Bangalore, India (CMU).
Call to Action
Ready to safeguard patient safety and elevate data integrity through centralized, risk‑based medical monitoring? Apply now for the Medical Reviewer role at Novo Nordisk before 31 July 2025.
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