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Medical Reviewer

0-2 years
Not Disclosed
10 March 19, 2025
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: Medical Reviewer - Clinical Trials
Location: Bangalore, India
Department: Centralised Monitoring Unit
Job Category: Clinical Development


Join Us as a Medical Reviewer in Clinical Trials

Are you passionate about ensuring high-quality medical data in clinical trials? Do you have a keen eye for detail and a drive to resolve medical concerns? If so, we have the perfect opportunity for you. Join our Centralised Monitoring Unit in Bangalore and contribute to life-changing research. Apply today for a rewarding career!


Position Overview:

As a Medical Reviewer at Novo Nordisk, you will be responsible for ensuring high-quality, consistent medical data for assigned clinical trials. Your responsibilities include:

  • Medical Review: Review all trial subjects in assigned clinical trials to ensure the consistency and quality of medical data.
  • Trial Planning: Participate in planning activities related to medical review.
  • Issue Resolution: Clarify and resolve medical concerns or inconsistencies in clinical trial data in collaboration with investigational site staff.
  • Reporting: Present findings from your medical review to relevant medical specialists to facilitate decision-making.
  • Documentation: Document the medical review in the sponsor’s Trial Master File (TMF).

Qualifications:

We are looking for candidates who meet the following criteria:

  • Educational Background: Postgraduate degree in medicine (preferably an MD in Pharmacology).
  • Experience: At least 2+ years of experience as a Medical Reviewer (preferred).
  • Knowledge:
    • Strong understanding of ICH GCP (International Council for Harmonisation Good Clinical Practice).
    • Good knowledge of medical terminology and clinical trial activities.
  • Technical Skills: Demonstrated proficiency with MS Office, MS Project, and PowerPoint.

About the Department:

The Centralised Monitoring Unit in Bangalore is a dynamic and collaborative team where you will work alongside dedicated professionals focused on ensuring the integrity and quality of clinical trial data. The team is committed to driving scientific communication strategies and building strategic relationships with key stakeholders. With a strong emphasis on medical education, we aim to make a meaningful impact on healthcare professionals and patients worldwide.


Why Novo Nordisk?

Novo Nordisk is a leading global healthcare company with a 100-year legacy of driving change to defeat chronic diseases. We are expanding our commitment to reach millions of people globally, impacting over 40 million patient lives daily. As one of the top 20 most valuable companies globally, we recognize the power of collaboration and diverse perspectives. At Novo Nordisk, we are working toward something bigger than ourselves—together, we go further. Together, we’re life-changing.


Contact:

If you are a match for the above qualifications and eager to take on this important role, please apply online through our application tool.


Deadline:

Apply on or before 21st March 2025.


Disclaimer:
Please be aware of fraudulent job offers. Novo Nordisk does not extend unsolicited offers or request payments during the recruitment process.