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Regional Medical Advisor - Insulin

2+ years
Not Disclosed
10 Feb. 24, 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

Position: Regional Medical Advisor - Insulin / Semaglutide
Location: Delhi, India
Job Category: Medical Affairs

Locations: Chandigarh, Delhi, Guwahati, Jaipur, Kochi, Kolkata, Lucknow, Mumbai, Pune


The Position:

Novo Nordisk is looking for an experienced Regional Medical Advisor to join our Medical Affairs Team. In this role, you will be responsible for implementing medical strategies and contributing to medico-marketing activities for insulin and semaglutide in your designated region. If you’re passionate about medical affairs and want to be part of a dynamic and growing environment, we want to hear from you.

Key responsibilities include:

  • Execution of Medical Strategy: Implement the Indian medical strategy into local activities within your region.

  • Relationship Building: Develop and maintain strong scientific relationships with key influencers and stakeholders.

  • Training & Education: Conduct training and educational programs for Physicians and Healthcare Professionals (HCPs) working with diabetes and obesity.

  • Medical Support: Provide medical support to the brand team, assisting in sharpening and positioning product strategies.

  • Market Insights: Stay updated on scientific knowledge, participate in scientific meetings, and gather feedback from key opinion leaders (KOLs) to inform internal stakeholders.

  • Advocacy Development: Build strong advocacy for Novo Nordisk’s portfolio through ongoing scientific interactions with external stakeholders.


Qualifications:

To be successful in this role, you should possess:

  • Education: An MBBS or MD in Pharmacology from a reputed institution. Alternatively, an MDS/BDS with at least 2 years of clinical work experience in medical affairs, clinical research, pharmacovigilance, or related fields.

  • Experience: Strong scientific knowledge in diabetes and obesity, including both the therapy area and the products. Good collaboration with both internal and external stakeholders.

  • Skills:

    • Strong communication and negotiation skills.

    • Analytical capabilities with a demonstrated ability to analyze complex situations.

    • Planning, execution, and follow-up skills.

    • A creative and innovative mindset to drive initiatives with operational excellence.


About the Department:

The Clinical, Medical, and Regulatory (CMR) department at Novo Nordisk is one of the most diverse and collaborative groups within the organization. CMR plays a key role in developing and implementing regulatory strategies, conducting HCP interactions, and ensuring patient-centered focus. As part of Novo Nordisk, you will help improve the quality of life for patients around the world.


Working at Novo Nordisk:

Novo Nordisk is a global leader in healthcare, with over 100 years of experience driving change to defeat serious chronic diseases. Building on our legacy in diabetes, we are expanding rapidly and reaching millions of patients worldwide. Our success is driven by over 63,000 employees collaborating across the globe. We believe in working towards something greater than ourselves, and together, we are life-changing.


Application Details:

Interested candidates are encouraged to submit their CV and motivational letter via the online application system.

Deadline: 26th February 2025