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International Medical Scientist

3+ years
Not Disclosed
10 Feb. 5, 2025
Job Description
Job Type: Full Time Education: MD/MBBS/PhD/DM 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: International Medical Scientist
Location: Bangalore, India
Department: Medical Data Review, Centralized Monitoring Unit - GBS
Job Category: Clinical Development


About the Role

Novo Nordisk is looking for an International Medical Scientist to drive the development of new therapeutic solutions and play a key role in transforming the lives of patients worldwide. In this role, you will collaborate closely with colleagues across the organization to contribute to planning, managing, and executing clinical trials, providing oversight during trial conduct, and ensuring the medical and scientific integrity of the clinical development program. This role offers a global perspective, requiring collaboration with stakeholders across countries and cultures.


Responsibilities

  • Clinical Development: Provide medical input to clinical development programs for phases 2-4, focusing on trial execution, monitoring, and ensuring data accuracy.
  • Medical Oversight: Manage medical aspects of trials, including handling medical queries, protocol deviations, and contributing to Investigator’s Brochure updates.
  • Medical Device Support: Contribute to risk management and medical input for device technical files and life-cycle management activities.
  • Cross-Department Collaboration: Coordinate with core teams (Medical Specialists, line managers, GPTs) to ensure alignment with clinical development goals.
  • Compliance and Audit Support: Support audit and inspections by managing medical monitoring audits and post-audit actions.

Qualifications

  • Required:
    • Medical Degree (MD/MBBS); advanced qualifications (PhD, DM) preferred.
    • Experience with cardiovascular & endocrine disorders.
    • Proven clinical development experience or roles such as Principal Investigator/Co-Investigator for Phase 2-3 trials.
    • Strong oral and written communication skills in English.
  • Preferred:
    • Experience in Pharma/Biotech companies, strategic planning, and managing clinical trials.
    • Strong collaboration and flexibility in a dynamic, fast-paced environment.

About the Department

The Medical Data Review team within the Centralized Monitoring Unit at Novo Nordisk is focused on driving innovation in the development of new medicines. The department thrives in a collaborative, fast-paced environment, committed to making a significant difference in patient lives.


About Novo Nordisk

Novo Nordisk is a global leader in healthcare, with over 100 years of expertise in transforming the treatment of chronic diseases. The company impacts the lives of millions worldwide, focusing on diabetes care while expanding its commitment to other critical diseases. As one of the most valuable companies globally, Novo Nordisk places great importance on diversity and collaboration, aiming to create a more inclusive and life-changing world.


How to Apply

Interested candidates can apply using Novo Nordisk’s online application tool.
Deadline: Apply on or before 10th February 2025.