Welcome Back

Google icon Sign in with Google
OR
I agree to abide by Pharmadaily Terms of Service and its Privacy Policy

Create Account

Google icon Sign up with Google
OR
By signing up, you agree to our Terms of Service and Privacy Policy
Instagram
youtube
Facebook

Associate Medical Reviewer

Novo Nordisk
Novo Nordisk
1-2 years
preferred by company
10 Jan. 20, 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

Job Title: Associate Medical Reviewer – Clinical Development
Location: Bangalore, Karnataka, India
Job Type: Full-Time
Experience Required: 1–2 Years in Clinical Practice or Academic Medical Field
Department: Central Monitoring Unit, Novo Nordisk Global Business Services (GBS), Bangalore


About Novo Nordisk

Novo Nordisk is a global healthcare leader dedicated to improving patient outcomes and advancing clinical research. With a focus on innovative therapies for chronic diseases, we combine a rich legacy of scientific excellence with a culture of curiosity, collaboration, and purpose-driven impact. Our Centralized Monitoring Unit (CMU) in Bangalore plays a vital role in ensuring the safety and quality of clinical trials by integrating medical expertise with cutting-edge data and statistical monitoring.


Role Overview

The Associate Medical Reviewer will play a critical role in clinical trial oversight, ensuring high-quality, consistent medical data while safeguarding patient safety. You will review trial data, monitor protocol compliance, and collaborate with multidisciplinary teams to deliver inspection-ready, high-quality outcomes.

Key Responsibilities:

  • Conduct medical reviews of clinical trial subjects to ensure protocol adherence, data accuracy, and patient safety in compliance with ICH GCP guidelines, local regulations, and SOPs.

  • Identify, analyze, and resolve data inconsistencies or clinically significant issues by collaborating with site staff and healthcare professionals.

  • Perform centralized medical monitoring, including evaluating outliers, assessing risk-based monitoring triggers, and providing actionable recommendations.

  • Document all review activities to maintain inspection-ready clinical trial records.

  • Present medical review findings to Medical Specialists to facilitate informed decision-making.

  • Stay current on therapeutic areas, protocol updates, and emerging medical developments relevant to assigned studies.

  • Collaborate closely with Data Managers, Trial Managers, and other team members to ensure timely, high-quality deliverables.


Required Qualifications

  • Graduate medical degree (MBBS + MD) with 1–2 years of clinical or academic experience.

  • Strong knowledge of ICH GCP guidelines, clinical trial protocols, and medical terminology.

  • Proficiency in computer applications, including MS Office, MS Project, and PowerPoint.

  • Experience in risk-based monitoring methodologies and familiarity with clinical trial data systems is preferred.

  • Excellent written and verbal English communication skills.

  • Strong analytical, problem-solving, and organizational skills with the ability to manage complex tasks independently.

  • Effective stakeholder management and collaboration skills.


About the Central Monitoring Unit (CMU)

The CMU Bangalore combines medical, technical, and statistical expertise to ensure patient safety and trial integrity. Medical Reviewers work alongside Medical Specialists, Functional Programmers, and Statistical Monitors to:

  • Ensure protocol compliance and identify clinically significant outliers.

  • Perform medical data cleaning and review.

  • Utilize operational visualizations and statistical monitoring tools to detect unusual patterns and potential compliance issues.

  • Collaborate globally to maintain high standards in clinical trial conduct.


Why Join Novo Nordisk

At Novo Nordisk, every team member contributes to transforming healthcare and improving patient lives worldwide. We offer:

  • Competitive compensation and benefits tailored for India-based employees.

  • Opportunities for professional growth and exposure to global clinical research.

  • A collaborative, innovative, and inclusive work culture.

  • Engagement in high-impact clinical trials advancing treatments for serious chronic diseases.

Join us to be part of a team where your medical expertise drives quality clinical outcomes and real-world patient impact.


Important Notes

  • Deadline for applications: 15th January 2026

  • Novo Nordisk does not solicit payments or personal information as part of its recruitment process. Beware of fraudulent offers.

  • Job titles may be updated during the recruitment process.


SEO & GEO Optimized Keywords:
Associate Medical Reviewer Bangalore, Clinical Data Medical Reviewer Jobs India, Clinical Trial Monitoring Careers, Medical Monitoring ICH GCP, Centralized Monitoring Unit Jobs, Novo Nordisk Clinical Research Careers