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International Medical Scientist

3+ years
Not Disclosed
10 Jan. 31, 2025
Job Description
Job Type: Full Time Education: MD/MBBS 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 | Novo Nordisk – Bangalore

💼 Company: Novo Nordisk
📍 Location: Bangalore, Karnataka, India
🕒 Job Type: Full-Time
📑 Category: Clinical Development

About Novo Nordisk

Novo Nordisk is a global leader in healthcare with a century-long legacy of transforming the treatment of chronic diseases. Specializing in diabetes care, Novo Nordisk is expanding its efforts to reach millions of people worldwide. As one of the 20 most valuable companies globally, Novo Nordisk is focused on creating a more inclusive world with a commitment to improving the lives of 40 million patients daily.

Position Overview

As an International Medical Scientist, you will be part of the Medical Data Review team in the Centralized Monitoring Unit based in Bangalore. Your work will contribute to clinical trials, medical research, and the development of life-changing therapeutic solutions for unmet patient needs. This role requires strong cross-cultural awareness and global collaboration, given the international scope of the position.

Key Responsibilities

💡 Clinical Development Program Management:

  • Provide medical input to clinical programs for phases 2-4.
  • Responsible for the medical oversight of clinical trials, managing queries, protocol deviations, and ensuring data accuracy.
  • Participate in Medical & Science Teams (MST) and safety committees to drive the progress of trials and resolve issues.

⚙️ Medical Device Support:

  • Offer expertise on risk management and medical device documentation.
  • Support the life-cycle management of medical devices.

📅 Medical Coordination:

  • Act as a liaison between core teams to ensure alignment with clinical development goals.

🔍 Compliance & Audits:

  • Manage medical monitoring audits and serve as a Subject Matter Expert (SME) during audits and inspections.

Qualifications

🎓 Education:

  • Medical Degree (MD/MBBS); advanced qualifications (PhD, DM) are preferred.
  • Experience working with Cardiovascular & Endocrine disorders.

💼 Experience:

  • Proven experience in clinical development for new molecules or roles like Principal Investigator in Phase 2-3 trials.
  • Experience in strategic planning and managing clinical trials in the pharmaceutical or medical device sector.

📝 Skills:

  • Strong communication and presentation skills in English.
  • High degree of independence and teamwork.
  • Ability to manage multiple tasks and stakeholders in a global environment.

Why Join Novo Nordisk?

Novo Nordisk offers an opportunity to be part of a global leader in healthcare, working with cutting-edge therapeutic solutions and having a real impact on patient lives. Join a diverse, inclusive team where your contributions help change the future of medicine.

How to Apply

Interested candidates are encouraged to apply via Novo Nordisk’s online application tool by 10th February 2025.

Note: Please be aware of fraudulent job offers. Novo Nordisk does not charge fees or request personal information during recruitment.