Location: Bengaluru, Karnataka, India
Company: Novo Nordisk Global Business Services (GBS)
Job Type: Full-Time
Work Mode: Onsite / Hybrid (As Per Business Requirement)
Industry: Clinical Research | Medical Monitoring | Clinical Development | Pharmaceutical | Healthcare
Department: Central Monitoring Unit (CMU) | Clinical Drug Development
Experience Required: 1–2 Years (Freshers Not Eligible)
Qualification Required: MBBS + MD
Novo Nordisk is hiring an Associate Medical Reviewer for its Central Monitoring Unit in Bengaluru. This opportunity is ideal for medical professionals with expertise in clinical research, medical monitoring, patient safety review, clinical trial data review, protocol compliance, centralized monitoring, and clinical data quality management.
The selected candidate will play a critical role in reviewing clinical trial medical data, identifying safety concerns, supporting protocol compliance, and ensuring high-quality, inspection-ready clinical trial documentation in collaboration with global clinical development teams.
This role is ideal for doctors seeking career growth in clinical development, medical monitoring, pharmaceutical research, clinical trial safety, and centralized medical review.
Ensure adherence to:
Collaborate closely with:
Support issue resolution and timely clinical decision-making.
The Central Monitoring Unit (CMU) at Novo Nordisk Bengaluru supports global clinical development through advanced centralized monitoring and medical review operations.
The team combines:
The unit collaborates globally to ensure patient safety, protocol compliance, data integrity, and high-quality clinical trial execution.
Candidates must have:
From a recognized medical institution.
Uttar Pradesh :
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