Senior Medical Reviewer – Clinical Drug Development
Location: Bangalore, Karnataka, India
Employment Type: Full-Time
Experience Required: 5+ years in clinical trial medical review or clinical monitoring
About Novo Nordisk Global Business Services (GBS), India:
Novo Nordisk GBS India in Bengaluru is a key hub supporting global clinical drug development. Our Centralised Monitoring Unit (CMU) focuses on risk-based medical monitoring, ensuring protocol compliance, high-quality clinical data, and patient safety across global trials. We collaborate closely with medical specialists, data managers, and technical programmers to deliver actionable insights and maintain inspection-ready clinical trial data.
Position Overview:
The Senior Medical Reviewer plays a pivotal role in the medical oversight of clinical trial data. This is a clinical data review role and not a pharmacovigilance position. The incumbent ensures the quality, consistency, and integrity of medical data across trials, identifies issues of medical concern, and facilitates timely resolution.
Key Responsibilities:
Conduct thorough medical reviews of clinical trial data to ensure patient safety, protocol adherence, and regulatory compliance.
Collaborate with study team members, including Data Managers, Trial Managers, and Medical Specialists, to maintain high-quality deliverables.
Identify and resolve medical data discrepancies and communicate findings to investigators and relevant medical specialists.
Document review outcomes in the Trial Master File (TMF) and ensure inspection readiness at all times.
Perform quality control of medical review tasks, ensuring consistency and accuracy.
Mentor and train new team members on therapeutic areas, processes, and best practices.
Contribute to process improvements and implementation of shared best practices.
Plan and manage resources for medical review tasks, including allocation and timeline management.
Qualifications and Experience:
MBBS with MD or equivalent; postgraduate specialization preferred.
Minimum 5 years of experience in clinical trial medical review or clinical monitoring.
Strong knowledge of ICH GCP guidelines and clinical trial regulations.
Experience with risk-based monitoring methodologies and clinical trial data systems.
Proficiency in MS Office, including MS Project and PowerPoint.
Excellent understanding of medical terminology and clinical trial operations.
Skills and Competencies:
Strong analytical, problem-solving, and result-oriented abilities.
Effective written and verbal communication skills in English.
Ability to independently plan and manage complex tasks.
Excellent stakeholder management and collaboration skills.
Attention to detail, high accuracy, and commitment to quality.
Why Join Novo Nordisk CMU:
Work at the forefront of clinical drug development, ensuring patient safety and data integrity.
Collaborate with global medical specialists and technical teams.
Engage in innovative, risk-based monitoring strategies for high-impact clinical trials.
Opportunity to contribute to process improvements and support inspection-ready clinical trial deliverables.
Application Deadline: 15th January 2026
Equal Opportunity Commitment:
Novo Nordisk is committed to inclusive recruitment and equality of opportunity. All qualified applicants are encouraged to apply.
Important Notice:
Novo Nordisk does not charge candidates fees or request payments during the recruitment process. Beware of fraudulent offers claiming to be from Novo Nordisk.
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