Novo Nordisk D Pharma Therapeutic Manager Job – Apply Online

Novo Nordisk D Pharma Therapeutic Manager Job – Apply Online

Novo Nordisk Pharma Job – Pharma Apply Online. Postgraduate and undergraduate pharma candidates apply. candidates are eligible to apply online for a Medical Information Therapeutic Manager post. Medical Information Therapeutic Manager position that is available at Novo Nordisk, which is one of the world’s most successful pharmaceutical companies

Job Title: Medical Information Therapeutic Manager

Qualifications
The right candidate for this position would possess below-mentioned requirements:

• Educational qualification: PhD, MBBS, Pharm D, M Pharm in Medical with a minimum of 2-3 years of relevant professional experience.
• Medical/Scientific writing experience in Diabetes/endocrinology /obesity or haemostasis is mandatory
• Detail-oriented with demonstrated editorial skills
• Literature search and assessment skills
• Prior experience in endocrinology, obesity or haemostasis therapy areas preferred..

About the Department

Global Medical Affairs, Bangalore (GMA-BLR), an extension of the Global Medical Affairs team in Headquarters in Denmark, is based out of Global Business Services (GBS), Bangalore, India. The team consists of highly motivated medical advisors, project managers and publication manager supporting HQ, regions and affiliates across the world.

The Position

As a Medical Information Therapeutic Manager, the key responsibilities include maintenance and updating a comprehensive library of

medical information (MI) responses for Novo Nordisk products. The job requires collaboration with internal stakeholders at the US Novo Nordisk affiliate office (NNI) to ensure consistent, accurate communication of MI in response to unsolicited inquiries from healthcare professionals, institutions and/or payors.

We expect you to create and/or revise standard and custom MI responses for use in responding to existing and anticipated medical and technical inquiries from health care professionals (HCPs). You must, participate in the approval process for custom and standard medical information responses to assure that all responses for a given brand are accurate, relevant and timely. Additionally, you should revise and/or add to content in comprehensive evidence-based medical information resources (e.g., clinical overviews, formulary dossiers, online evidence repository).

Apply Online

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