Novo Nordisk

Drug Safety Specialist

Novo Nordisk

Clayton, NC, USA
Full-TimeDepends on ExperienceSenior LevelMasters
Job Description

Welcome to Novo Nordisk, a global healthcare company with a passion for improving the lives of millions of people worldwide. We are currently seeking a highly skilled and motivated Drug Safety Specialist to join our team. As a Drug Safety Specialist, you will play a crucial role in ensuring the safety and efficacy of our pharmaceutical products. Your expertise and attention to detail will be instrumental in helping us maintain our commitment to patient safety and compliance. If you are dedicated, detail-oriented, and have a strong understanding of pharmacovigilance and drug safety regulations, we encourage you to apply for this exciting opportunity. Come join us in making a difference in the lives of patients around the world.

  1. Conduct thorough and timely review of adverse event reports for Novo Nordisk products.
  2. Adhere to all relevant pharmacovigilance regulations and company policies.
  3. Collaborate with cross-functional teams to ensure accurate and timely reporting of adverse events.
  4. Monitor and analyze safety data to identify potential trends or safety signals.
  5. Participate in the development and implementation of risk management plans for Novo Nordisk products.
  6. Communicate with regulatory agencies and business partners regarding drug safety matters.
  7. Conduct safety assessments and prepare safety reports for regulatory submissions.
  8. Serve as a subject matter expert on drug safety processes and regulations.
  9. Support drug safety audits and inspections.
  10. Provide training and guidance to colleagues on drug safety processes and procedures.
  11. Continuously monitor and evaluate drug safety processes to identify areas for improvement.
  12. Maintain accurate and complete documentation of all drug safety activities.
  13. Stay updated on industry developments and changes in drug safety regulations.
  14. Represent Novo Nordisk at conferences and meetings related to drug safety.
  15. Maintain a high level of confidentiality and professionalism in handling sensitive information.
Where is this job?
This job is located at Clayton, NC, USA
Job Qualifications
  • Bachelor's Degree In Pharmacy, Pharmaceutical Sciences, Or Related Field.

  • Minimum Of 2 Years Of Experience In Drug Safety Or Pharmacovigilance.

  • Knowledge Of Fda And International Drug Safety Regulations And Guidelines.

  • Strong Analytical Skills And Attention To Detail.

  • Excellent Communication And Interpersonal Skills, With The Ability To Work In A Cross-Functional Team Environment.

Required Skills
  • Risk Management

  • Data Analysis

  • Drug development

  • Medical Terminology

  • Regulatory compliance

  • pharmacology

  • Clinical Trials

  • Drug Safety

  • Pharmacovigilance

  • Safety Reporting

  • Adverse Events

Soft Skills
  • Communication

  • Conflict Resolution

  • Emotional Intelligence

  • Leadership

  • Time management

  • creativity

  • Teamwork

  • Adaptability

  • Problem-Solving

  • Empathy

Compensation

According to JobzMall, the average salary range for a Drug Safety Specialist in Clayton, NC, USA is between $60,000-$90,000 per year. However, this may vary depending on the specific company, level of experience, and additional skills and qualifications. Some Drug Safety Specialists may earn higher salaries, up to $120,000 or more, with more experience and advanced certifications.

Additional Information
Novo Nordisk is an Equal Opportunity Employer. We celebrate diversity and are committed to creating an inclusive environment for all employees. We do not discriminate based upon race, religion, color, national origin, sex, sexual orientation, gender identity, age, status as a protected veteran, status as an individual with a disability, or other applicable legally protected characteristics.
Required LanguagesEnglish
Job PostedMarch 29th, 2024
Apply BeforeMay 22nd, 2025
This job posting is from a verified source. 
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About Novo Nordisk

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.

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