Pharmacovigilance Technology Professional

The position

Joining our team means engaging in day-to-day responsibilities while also contributing to various projects. In this temporary position, you will collaborate with dedicated colleagues and have exceptional opportunities for professional growth in a flexible environment where you can support multiple processes. We aim to hire two candidates for this position, starting on 1 August , with an end date of 31 December . As a Pharmacovigilance Technology Professional, you will work alongside your team to support the continuous improvement, development, and maintenance of the global safety database, ensuring the daily processing and submission of Individual Case Safety Reports (ICSRs). Key responsibilities will include: Monitoring the department mailbox Configuring the safety database (code lists, clinical trials, etc.) Front-end troubleshooting, incident reporting, end-user support, and identifying improvement initiatives Participating in cross-organizational projects and relevant working groups as necessary Maintaining and updating standard operating procedures This role provides an opportunity to work both independently and collaboratively with highly skilled colleagues. Taking on responsibility, effective communication, and proactive decision-making will be essential components of your daily work. Qualifications As an ideal candidate, you should have the following qualifications: A relevant university degree, such as in biomedicine or computer science Experience in drug safety/pharmacovigilance, either through case processing or database configuration, and a strong willingness to learn and adapt Experience in stakeholder management and end-user support, including troubleshooting Ethical conduct, proactivity, and strong organizational skills Fluent in both written and spoken English (company language) We are looking for a colleague who will thrive collaborating effectively in a multicultural and dynamic environment. About the Department With 25 highly dedicated team members based in Denmark and India, the team bears global responsibility for supporting, maintaining and continually enhancing the global safety database. Presently, we are in the midst of transitioning to a new safety database and clinical safety database, which may be pertinent for candidates based on their individual qualifications. Depending on your individual qualifications, you may be assigned to work with the database that aligns best with your experience. Working at Novo Nordisk At Novo Nordisk, we do not wait for change. We drive it. We are a dynamic company in an even more dynamic industry, and we know that what got us to where we are today is not necessarily what will make us successful in the future. We embrace the spirit of experimentation, striving for excellence without fixating on perfection. We never shy away from opportunities to develop, we seize them. From research and development, through to manufacturing, marketing, and sales – we are all working to move the needle on patient care.