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International Medical Scientist

3+ years
Not Disclosed
10 Jan. 16, 2025
Job Description
Job Type: Full Time Education: MBBS/MD/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

 


International Medical Scientist

Category: Clinical Development
Location: Bangalore, Karnataka, India


Department

Medical Data Review, Centralized Monitoring Unit – Bangalore, GBS


Job Overview

Are you driven by the opportunity to transform patients' lives globally with innovative therapeutic solutions? Are you passionate about clinical trials and medical research? If so, Novo Nordisk invites you to join our team as an International Medical Scientist. This position provides a unique opportunity to drive drug development efforts, ensuring optimal patient care for those with the greatest unmet needs.


The Position

As an International Medical Scientist, you will collaborate closely with Novo Nordisk colleagues worldwide.

Key Responsibilities

  • Clinical Development Program
    • Contribute medical insights to Phase 2–4 clinical programs.
    • Oversee clinical trial conduct, address medical queries, protocol deviations, and ensure data accuracy via medical monitoring.
  • Medical Oversight
    • Manage delegated projects, resolve trial-related issues, and participate in safety committees.
    • Update the Investigator’s Brochure and review clinical trial reports.
  • Medical Device Support
    • Provide risk management input and contribute to the medical device lifecycle documentation.
  • Medical Coordination
    • Act as a liaison between teams to align clinical development goals.
  • Compliance Support
    • Lead audits, inspections, and post-audit actions as a Subject Matter Expert (SME).

Qualifications

  • Education: Medical Degree (MD/MBBS); advanced degrees (PhD/DM) preferred, with expertise in Cardiovascular and Endocrine disorders.
  • Experience:
    • Proven track record in clinical development or roles like Principal Investigator/Co-Investigator for Phase 2–3 trials.
    • Industry experience in Pharma/Biotech, strategic planning, and trial management.
  • Skills:
    • Strong communication and presentation abilities in English.
    • Proficiency in strategic and operational clinical research methodologies.

Key Attributes

  • Open-minded and innovative with strong collaboration skills.
  • High independence and team spirit.
  • Ability to manage multiple tasks and stakeholders with focus and flexibility.

About the Department

You will join the Medical Data Review Team in the Centralized Monitoring Unit based in Bangalore. This dynamic team of professionals drives excellence in the development of life-changing medicines.


Working at Novo Nordisk

Novo Nordisk is a global healthcare leader with a 100-year legacy of transforming chronic disease management. Reaching over 40 million patients daily, we are driven by our commitment to making a difference. With over 63,000 employees worldwide, we foster an inclusive culture that celebrates diversity and empowers our team to go further together.


Application Details

  • Deadline: 23rd January 2025
  • Contact: Apply via Novo Nordisk’s online application tool.

Important Notice

Beware of fraudulent job offers. Novo Nordisk does not charge fees or request funds during the recruitment process.


Join Us

Together, we’re life-changing. Apply today and contribute to our mission of shaping the future of healthcare.