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Associate Medical Reviewer

Novo Nordisk
Novo Nordisk
1-2 years
Not Disclosed
Bengaluru, Karnataka, India
10 March 27, 2026
Job Description
Job Type: Full Time Education: B.Sc./ M.Sc./ M.Pharm/ B.Pharm/ Life Sciences Skills: Causality Assessment, Clinical SAS Programming, Communication Skills, CPC Certified, GCP guidelines, ICD-10 CM Codes, CPT-Codes, HCPCS Codes, ICD-10 CM, CPT, HCPCS Coding, ICH guidelines, ICSR Case Processing, Interpersonal Skill, Labelling Assessment, MedDRA Coding, Medical Billing, Medical Coding, Medical Terminology, Narrative Writing, Research & Development, Technical Skill, Triage of ICSRs, WHO DD Coding

Associate Medical Reviewer – Clinical Trial Data Review & Medical Monitoring

Location: Bengaluru, Karnataka, India
Company: Novo Nordisk
Department: Central Monitoring Unit (Clinical Development – GBS)
Job Type: Full-Time

Experience Required: 1–2 years (Clinical practice or academic experience)

Educational Qualification: MBBS with MD (mandatory)

Overview
Novo Nordisk is seeking a highly motivated Associate Medical Reviewer to join its Central Monitoring Unit in Bengaluru. This role is designed for medical professionals passionate about clinical research, patient safety, and high-quality data review. As part of a global clinical development team, you will contribute to ensuring the integrity, consistency, and compliance of clinical trial data while supporting innovative drug development programs.

Key Responsibilities
The Associate Medical Reviewer will conduct comprehensive medical reviews of clinical trial subjects to ensure accuracy, consistency, and adherence to study protocols. You will play a critical role in safeguarding patient safety by evaluating clinical data in line with Good Clinical Practice (GCP), ICH guidelines, and local regulatory requirements.

The role involves identifying clinically significant inconsistencies, outliers, or safety concerns in trial data and collaborating with investigators, site staff, and healthcare professionals to resolve them. You will perform medical monitoring activities, including protocol compliance checks and data validation, while ensuring that all review activities are properly documented for audit and inspection readiness.

Additionally, you will present findings to Medical Specialists to support informed decision-making and work closely with cross-functional teams such as Data Management, Trial Management, and Statistical Monitoring to deliver high-quality outcomes. Continuous learning and staying updated on therapeutic areas and clinical trial methodologies are essential aspects of this role.

Required Skills and Competencies
Candidates should have a strong understanding of clinical trial processes, medical terminology, and regulatory frameworks including ICH-GCP guidelines. Familiarity with risk-based monitoring approaches and clinical data systems is highly desirable.

Strong analytical thinking, attention to detail, and the ability to interpret complex clinical data are critical for success. Excellent written and verbal communication skills, along with the ability to manage stakeholders and work independently, are essential. Proficiency in MS Office tools such as Excel, PowerPoint, and Project is expected.

About the Team
The Central Monitoring Unit in Bengaluru operates as a collaborative hub of medical reviewers, statisticians, and technical experts working together to ensure clinical trial quality and patient safety. The team partners closely with global stakeholders to identify data trends, detect anomalies, and enhance study outcomes through centralized monitoring strategies.

Why Join Novo Nordisk
Novo Nordisk offers a purpose-driven work environment focused on advancing treatments for chronic diseases. Employees benefit from a strong culture of innovation, collaboration, and continuous learning, with opportunities to contribute to global clinical research initiatives that impact millions of lives.

Application Deadline: 15 January 2026

This is an excellent opportunity for early-career medical professionals to transition into clinical research and medical monitoring, gaining global exposure in clinical development and regulatory-compliant data review.