Pharmacovigilance Specialist

Are you passionate about patient safety and making a difference in the pharmaceutical industry? Do you have a keen eye for detail and excellent analytical skills? Novo Nordisk is seeking a highly motivated and experienced Pharmacovigilance Specialist to join our team. As a global leader in diabetes care, our company is committed to ensuring the safety and efficacy of our products. If you have a strong background in pharmacovigilance and a desire to contribute to improving patient outcomes, we invite you to apply for this exciting opportunity.

1. Monitor and analyze safety data for Novo Nordisk products to ensure compliance with regulatory requirements and company standards.
2. Conduct thorough and timely review of adverse event reports, product quality complaints, and other safety-related information.
3. Collaborate with cross-functional teams to ensure appropriate and timely reporting of safety data to regulatory authorities.
4. Identify and investigate potential safety signals and escalate to management as needed.
5. Develop and maintain comprehensive pharmacovigilance processes and procedures in accordance with company policies and regulations.
6. Stay updated on relevant regulations, guidelines, and industry best practices related to pharmacovigilance.
7. Serve as a subject matter expert for pharmacovigilance and provide guidance and training to other team members.
8. Contribute to the development and implementation of risk management plans for Novo Nordisk products.
9. Participate in pharmacovigilance audits and inspections, providing necessary documentation and support.
10. Continuously evaluate and improve pharmacovigilance processes to ensure the highest level of patient safety.
11. Collaborate with internal and external stakeholders to ensure effective communication and collaboration on pharmacovigilance activities.
12. Prepare and present periodic safety reports and other safety-related documents to internal and external audiences.
13. Act as a key point of contact for safety-related inquiries and requests from regulatory authorities, healthcare professionals, and patients.
14. Proactively identify and communicate potential safety issues to relevant stakeholders and contribute to risk management strategies.
15. Maintain accurate and up-to-date pharmacovigilance databases and systems.
16. Contribute to the development and implementation of pharmacovigilance training programs for internal staff and external partners.
17. Adhere to all applicable laws, regulations, and company policies related to pharmacovigilance.
18. Participate in various cross-functional projects and initiatives related to patient safety and pharmacovigilance.
19. Represent Novo Nordisk at external meetings, conferences, and events related

According to JobzMall, the average salary range for a Pharmacovigilance Specialist in Princeton, NJ, USA is between $70,000-$110,000 per year. This can vary depending on factors such as experience, qualifications, and the specific company or organization they work for.

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.