Apply for Senior Drug Safety Associate at Novo Nordisk- Apply before 24th January 2024

Novo Nordisk

Website Novo Nordisk

About Novo Nordisk

Novo Nordisk is indeed a renowned global healthcare company with a remarkable 89-year history of innovation and leadership in the field of diabetes care. The company has consistently been at the forefront of diabetes treatment and research, making significant contributions to improving the lives of people living with diabetes.

In addition to their pioneering work in diabetes care, Novo Nordisk has established leading positions in other critical areas of healthcare. This includes Haemophilia care, where they have developed and provided advanced therapies to manage this complex bleeding disorder. They are dedicated to improving the quality of life for individuals with Haemophilia.

Novo Nordisk is also a leader in the field of growth hormone therapy, offering innovative solutions for individuals with growth-related disorders. Their commitment to research and development has allowed them to make significant strides in this area.

Furthermore, the company plays a vital role in hormone replacement therapy, which is essential for individuals who require replacement hormones due to various medical conditions. Novo Nordisk’s expertise and products in this field have helped countless patients achieve a better quality of life.

Overall, Novo Nordisk’s longstanding commitment to innovation and its leadership in multiple healthcare sectors, particularly in diabetes care, Haemophilia care, growth hormone therapy, and hormone replacement therapy, have made it a globally respected and trusted healthcare company. Their work continues to have a positive impact on the health and well-being of millions of people worldwide.

Job Description

The Position

We are seeking a Senior Drug Safety Associate to conduct initial evaluations of reported adverse events from diverse sources. Key responsibilities include case entry and verification, causality assessment, and ensuring accurate safety information in the Novo Nordisk safety database. Timely follow-up requests and queries, as well as weekly literature surveillance, are integral to the role.

About the Department

Join the Global Safety Global Business Service (GS-GBS) team, established in 2010 as a hub for safety case processing. Engage in diverse activities such as safety case processing, medical review, safety surveillance, medical writing, report submission, training, quality control, and literature surveillance.

Candidate Profile

  • Graduation and/or post-graduation in life sciences.
  • Profound knowledge of Pharmacovigilance.
  • Familiarity with medical terminologies and clinical pharmacology.
  • Strong understanding of internal and external Pharmacovigilance settings.
  • Proficient in MS Windows applications, including MS Office tools.
  • Solid understanding of Novo Nordisk’s organizational or pharmaceutical company structure.
  • Excellent written and oral communication skills in English.
  • In-depth knowledge of Novo Nordisk products, mechanism of action, safety profile, etc.
  • Good understanding of GXP requirements.

Additional Information

  • Qualification:

    Graduation and/or post-graduation in life sciences

  • Location:

    Bangalore, Karnataka

  • Industry Type:

    Pharma/ Healthcare/ Clinical research

  • Functional Area:

    Reg Affairs & Safety Pharmacovigilance

  • End Date:

    24th January 2024

Apply Online

Apply Now

To apply for this job please visit careers.novonordisk.com.