Pharmacovigilance Specialist

At Novo Nordisk, we are committed to improving the lives of millions of people living with chronic diseases. As a Pharmacovigilance Specialist, you will play a crucial role in ensuring the safety and efficacy of our life-saving medications. We are looking for a highly skilled and motivated individual who is passionate about patient safety and has a strong understanding of drug safety regulations. If you are dedicated, detail-oriented, and have a desire to make a positive impact in the healthcare industry, we want you on our team. Join us at Novo Nordisk and be a part of a company that is making a difference in the lives of patients around the world.

1. Monitor and evaluate the safety and efficacy of Novo Nordisk's medications through the collection, analysis, and reporting of adverse events and product complaints.
2. Conduct thorough investigations of adverse events and product complaints, working closely with cross-functional teams to gather relevant information and ensure timely and accurate reporting to regulatory authorities.
3. Stay up-to-date on drug safety regulations and guidelines to ensure compliance with applicable local and international laws.
4. Collaborate with internal and external stakeholders, including regulatory authorities, healthcare professionals, and patients, to ensure timely and accurate communication of safety information.
5. Develop and maintain standard operating procedures, processes, and training materials related to pharmacovigilance.
6. Participate in the review and approval of promotional materials to ensure compliance with safety regulations.
7. Contribute to the development and maintenance of risk management plans for Novo Nordisk's medications.
8. Conduct signal detection activities to identify any potential safety concerns and make recommendations for further evaluation.
9. Support the preparation and submission of safety reports to regulatory authorities, including periodic safety update reports and signal detection reports.
10. Act as a subject matter expert on pharmacovigilance and provide guidance and support to other departments within the company.
11. Participate in audits and inspections related to pharmacovigilance and ensure timely and appropriate follow-up on any findings.
12. Continuously evaluate and improve pharmacovigilance processes and systems to ensure the highest level of patient safety.
13. Represent Novo Nordisk at conferences and meetings related to drug safety and pharmacovigilance.
14. Maintain confidentiality and adhere to ethical standards in all aspects of work.
15. Uphold Novo Nordisk's commitment to improving the lives of patients living with chronic diseases.

According to JobzMall, the average salary range for a Pharmacovigilance Specialist in Munich, Germany is between €50,000 and €70,000 per year. However, this can vary depending on the specific company, experience level, and qualifications of the individual. Some companies may offer higher salaries for those with advanced degrees or specialized skills in pharmacovigilance. Additionally, salaries may increase with experience and additional responsibilities within the role.

Novo Nordisk AS engages in the research, development, manufacture, and marketing of pharmaceutical products. It operates through the Diabetes and Obesity Care; and Biopharmaceuticals segments. The Diabetes and Obesity Care segment covers insulins, glucagon-like-peptide 1, other protein-related products, oral anti-diabetic drugs and obesity. The Biopharmaceuticals segment handles the research, development, manufacture, and distribution of products within the areas of haemophilia, growth hormone, hormone replacement, inflammation and other therapy areas.