
Pharmacovigilance Specialist
Hello and welcome to Novo Nordisk! We are currently seeking a highly skilled Pharmacovigilance Specialist to join our team. As a global healthcare company, our mission is to improve the lives of millions of people through innovative and life-saving treatments. As a Pharmacovigilance Specialist, you will play a crucial role in ensuring the safety and efficacy of our products. We are looking for a driven and detail-oriented individual with a strong background in pharmacovigilance and a passion for making a difference in patient's lives. If you are ready for a challenging and rewarding career with a company that values innovation and patient care, then we encourage you to apply for this role.
- Conduct and oversee all aspects of pharmacovigilance activities, including case processing, assessment, and reporting of adverse events.
- Stay up-to-date with global regulations and guidelines related to pharmacovigilance and ensure compliance within the company.
- Collaborate with cross-functional teams to develop and implement risk management plans for products.
- Conduct regular safety assessments and signal detection to identify potential safety concerns.
- Prepare and review safety reports for regulatory submissions.
- Conduct and oversee safety surveillance activities, including literature review and signal detection.
- Serve as the primary point of contact for safety-related inquiries from internal and external stakeholders.
- Train and mentor junior pharmacovigilance staff.
- Participate in cross-functional teams to support the development and launch of new products.
- Represent the company in safety discussions with regulatory authorities and participate in inspections and audits.
- Continuously monitor and evaluate the effectiveness of pharmacovigilance processes and make recommendations for improvements.
- Maintain a high level of accuracy and attention to detail in all pharmacovigilance activities.
- Adhere to strict timelines for reporting and responding to safety issues.
- Collaborate with medical affairs and clinical teams to ensure safety information is accurately communicated to healthcare professionals and patients.
- Maintain confidentiality and handle sensitive information in accordance with company policies and regulatory requirements.
Bachelor's Degree In Pharmacy, Life Sciences, Or A Related Field.
Minimum Of 2-3 Years Of Experience In Pharmacovigilance Or Drug Safety In The Pharmaceutical Industry.
In-Depth Knowledge Of Global Pharmacovigilance Regulations And Guidelines, Including Ich, Fda, And Ema Requirements.
Strong Analytical And Problem-Solving Skills, With The Ability To Effectively Evaluate And Report Safety Data.
Excellent Communication And Interpersonal Skills, With The Ability To Work Collaboratively With Cross-Functional Teams And External Stakeholders.
Risk Management
Risk assessment
Medical Writing
Drug Safety
Safety Reporting
Safety Surveillance
Signal Detection
Adverse Events
Case Processing
Pharmacovigilance Regulations
Signal Evaluation
Communication
Conflict Resolution
Emotional Intelligence
Leadership
Time management
Interpersonal Skills
creativity
Teamwork
Adaptability
Problem-Solving
According to JobzMall, the average salary range for a Pharmacovigilance Specialist in Zürich, Switzerland is between CHF 80,000 and CHF 130,000 per year. This range may vary depending on factors such as experience, education, and the specific company or organization the specialist is working for.
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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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