Novo Nordisk Therapeutic Manager Job – Pharma Candidates
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 In Global Medical Affairs
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
We are searching for a dynamic and outgoing team player who is able to perform in a highly dynamic, challenging and diverse environment, can communicate with clarity, able to carry tasks under pressure and deliver quality results on time. Also, you must possess a high level of business acumen, excellent stakeholder management and communication skills, including scientific communication, data analysis and interpretation.
Candidates for the position will need a high level of proficiency in verbal and written English and must be able to travel internationally (approximately 10%).
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 the content in comprehensive evidence-based medical information resources (e.g., clinical overviews, formulary dossiers, online evidence repository)
Furthermore, we expect you to ensure compliance with FDA requirements as they affect Medical Communications; responses must be accurate, up-to-date, balanced, and scientific. You will provide medical accuracy review for Promotional Review Board pieces containing relevant medical content.
You will work closely with the US Medical Information team and Global Medical Affairs team at Bangalore.
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