Experienced Safety Surveillance Advisers

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Søborg

Would you like to work in a global setting and play a key role in ensuring highest safety and lowest possible risk to patients that use Novo Nordisk products? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark? Then this is your unique opportunity to be our new colleague in Safety Surveillance. Join us and experience a world of opportunities. Apply now! The position We are currently expanding our clinical activities and we are therefore looking for experienced Safety Surveillance Advisers, who can support the ongoing safety surveillance of products in clinical development stage II & III as well as for marketed products. Key responsibilities include:
  • Perform critical analysis and medical evaluation of the emerging aggregate safety data and contribute to establishment of the product safety profile during development and post-marketing stages
  • Participate in preparation of communication about the benefit risk assessment (e.g., via Periodic Safety Update Reports, Development Safety Update Reports and Risk Management Plans)
  • Contribute to development of clinical trial protocols and clinical trial reports by using your medical/clinical expertise on collection and assessment of safety information
  • Represent Safety Surveillance in cross-functional teams
  • Potentially chair the internal Novo Nordisk safety committee for one or more products
    • You will get the opportunity both to work independently and in collaboration with a team of highly skilled, committed, and enthusiastic colleagues. Assuming responsibility, communicating information and taking action will be essential parts of your workday. You will have a close collaboration and interaction with other functional areas in Novo Nordisk especially the Non-clinical, Clinical Development and Regulatory Affairs team and it will give you an extensive insight to the whole Novo Nordisk value-chain. Qualifications As an ideal candidate, you have:
  • University degree in Medicine, Veterinary Medicine, Pharmacy or Biological Sciences
  • Several years of experience within drug safety/pharmacovigilance or drug development
  • Good understanding of medical concepts, disease processes, scientific methodology and data analysis
  • Strong IT skills and knowledge of computer systems
  • 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 thrive in in a fast-paced environment in continuous development and you are good at establishing contact, collaborating, and communicating with stakeholders. Additionally, you are a strong driver and a dedicated team player who enjoys a multicultural environment of continuous development. 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. We treasure a positive and inclusive atmosphere in our team(s) 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 Cecilie Freddie Lange at +45 3079 4908 or Kamilla Kjær Frederiksen at +45 3077 6794. Deadline 09 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. Please briefly explain what motivated you to apply for this role. Include your statement either in CV or Cover Letter if there is one. 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 17.3.2023, men kan have været deaktiveret og genaktiveret igen.

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    Dagligt opdateret: Dette job opdateres dagligt ud fra jobudbyderens hjemmeside via vores søgemaskineteknologi og er aktivt lige nu.
    • Forretningsudvikler
    • Søborg
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