Location: Bengaluru, Karnataka, India
Department: Central Monitoring Unit (CMU), Global Business Services
Company: Novo Nordisk
Application Deadline: 8th May 2026
About the Role
Are you looking to build a career in clinical research and medical monitoring while directly contributing to patient safety? The Associate Medical Reviewer role offers a high-impact opportunity to work on global clinical trials, ensuring data quality, protocol compliance, and subject safety. This position is ideal for medical professionals aiming to transition into the clinical research and pharmaceutical industry.
Key Responsibilities
Perform comprehensive medical review of clinical trial subjects to ensure accuracy, consistency, and quality of clinical data
Ensure patient safety and strict adherence to study protocols, ICH-GCP guidelines, and regulatory standards
Identify, evaluate, and resolve medical inconsistencies or safety concerns in collaboration with investigators and site teams
Conduct medical monitoring activities including protocol compliance checks and identification of clinically significant outliers
Present medical review insights to Medical Specialists to support data-driven decision-making
Maintain detailed documentation of all review activities to ensure audit and inspection readiness
Collaborate cross-functionally with Data Management, Trial Management, and Medical teams for seamless study execution
Stay updated with therapeutic knowledge, clinical protocols, and evolving regulatory requirements
Required Qualifications
MBBS with MD (mandatory)
1–2 years of experience in clinical practice or academic research
Experience Level: Entry-Level to Early Career (Freshers with MD qualification may be considered based on relevant exposure)
Required Skills and Competencies
Strong knowledge of ICH-GCP guidelines and clinical trial processes
Proficiency in MS Office tools including Excel, PowerPoint, and Project
Solid understanding of medical terminology and clinical data review
Familiarity with risk-based monitoring methodologies and clinical data systems
Excellent analytical thinking and problem-solving abilities
Strong communication, documentation, and stakeholder management skills
Ability to manage multiple priorities and work independently in a fast-paced environment
About the Department
The Central Monitoring Unit (CMU) at Bengaluru is an integral part of global clinical drug development operations. The team comprises Medical Reviewers, Functional Programmers, and Statistical Monitors working collaboratively to ensure clinical trial quality and patient safety.
Medical Reviewers work closely with global stakeholders to detect clinical risks, ensure protocol adherence, and enhance data integrity. This integrated model enables proactive monitoring, efficient data cleaning, and early identification of compliance issues in clinical trials.
Why Join Novo Nordisk
Work with a globally respected pharmaceutical leader with over 100 years of legacy
Contribute to innovative clinical research addressing serious chronic diseases
Exposure to global clinical trial processes and cross-functional collaboration
Strong focus on employee development, learning, and long-term career growth
Inclusive, purpose-driven, and innovation-focused work culture
Important Note for Applicants
This role is suitable for candidates with an MD qualification and foundational clinical experience. Candidates transitioning from clinical practice to the pharmaceutical or clinical research industry will find this role highly relevant.
How to Apply
Interested candidates are encouraged to apply before the deadline. For more verified global clinical research and pharmacovigilance job opportunities, visit ThePharmaDaily.com
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