Experienced Safety Surveillance Advisers
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Søborg
Would you like to be part of a department of highly skilled pharmacovigilance professionals? Do you possess a natural curiosity and analytical mindset, and are passionate about ensuring the safety and well-being of patients using Novo Nordisk products? If so, we invite you to consider joining our Safety Surveillance Obesity & NASH 1 team. Our organization is expanding, and we are seeking experienced Safety Surveillance Advisers for multiple senior/specialist positions. Apply now! The Position In this role, along with other colleagues, you will be responsible for ongoing safety surveillance of products in clinical development programs within weight management, liver disease, and other therapeutic areas. This role offers a unique chance to embark on a new and exciting area of work and contribute to the improvement of patient outcomes. Key responsibilities include: Represent Safety Surveillance in clinical development activities Perform critical analysis and medical evaluation of the emerging aggregate safety data and contribute to establishment of the product safety profile during development Participate in preparation of communication about the benefit risk assessment Represent Safety Surveillance in cross-functional teams Potentially chair the internal Novo Nordisk safety committee for one or more products In this role, you will have the unique opportunity to work both independently and collaboratively with a team of highly skilled, dedicated, and enthusiastic colleagues. Effective communication, assuming responsibility, and taking decisive action will be critical aspects of your daily work. Furthermore, you will work closely with other functional teams within Novo Nordisk, especially Non-clinical, Clinical Development, and Regulatory Affairs teams. This collaboration will provide you with extensive insights into the workings of our entire organisation. Qualifications We are looking for candidates with: Master’s degree in Medicine, Veterinary Medicine, Pharmacy or Biological Sciences or relevant Hands-on experience within drug safety/pharmacovigilance or drug development Good understanding of medical concepts, disease processes, scientific methodology and data analysis Experience with clinical trial activities and/or documented scientific training (e.g., PhD) will be an advantage As a person, you are ethical, responsible, well-organised and a strong communicator. You can work independently and under pressure when needed. You are a strong collaborator and a dedicated team player who thrives in a multicultural environment of continuous development. Additionally, you are good at establishing contact and collaborating with stakeholders. Finally, you are fluent in English both written and spoken (company language) and an experienced user of MS Office. About the department Safety Surveillance is a department within Global Safety situated in Søborg, Denmark. We are globally responsible for surveillance of all safety information for Novo Nordisk’s products that are currently marketed or under development. Our team currently consists of approximately 11 great employees with diverse educational backgrounds and broad international representation. We treasure a positive and inclusive atmosphere in our team and count on you to engage and participate in a positive manner as well. 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. Contact For further information please contact Marie Louise Muus Ghorbani at +45 3079 7790 or Britt Jørgensen at +45 3077 7660. Deadline Please apply for the positions no later than 10 April 2023. We will review the applications on an ongoing basis, so we encourage you to apply as soon as possible. We are looking for several similar profiles at Novo Nordisk now. Therefore, Hiring Managers from different teams might also look at your application. To ensure an efficient and fair recruitment process, please refrain from adding a photo in your CV. We commit to an inclusive recruitment process and equality of opportunity for all our job applicants. At Novo Nordisk we recognize that it is no longer good enough to aspire to be the best company in the world. We need to aspire to be the best company for the world and we know that this is only possible with talented employees with diverse perspectives, backgrounds and cultures. We are therefore committed to creating an inclusive culture that celebrates the diversity of our employees, the patients we serve and communities we operate in. Together, we’re life changing.
Information og data
Denne ledige stilling har jobtypen "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 24.3.2023, men kan have været deaktiveret og genaktiveret igen.
Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
- Forretningsudvikler
- Søborg
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