Experienced Surveillance Advisor within Medical Devices
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Søborg
Do you have a background working with medical devices? Would you like to be part of a department of highly talented pharmacovigilance professionals? Are you known for your innate curiosity and analytical mindset? If you are eager to play a pivotal role in ensuring the safety of our medical devices, we invite you to join our Safety Surveillance department at Novo Nordisk. Apply now and become an integral part of our mission! The position As an Experienced Safety Surveillance Adviser within the medical device area, you will together with other colleagues be responsible for the ongoing safety surveillance of all Novo Nordisk medical devices, from prefilled products to durable devices to software. Key responsibilities include: Perform critical analysis and medical evaluation of the emerging aggregate safety data received from sites participating in our clinical trials, or from patients or prescribers using a marketed product. Monitor post-marketing data to identify new signals and manage established risks. Participate in preparation of communication about the benefit risk assessment. Contribute to development of clinical trial protocols and clinical trial reports. Represent Safety Surveillance in cross-functional teams. 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 a cornerstone of your workday. You can expect a close collaboration with other functional areas in Novo Nordisk (such as Medical and Science and Regulatory Affairs) which will give you an extensive insight to the whole Novo Nordisk device organisation. Qualifications To thrive in this role, you need to have: University degree in Medicine, Veterinary Medicine, Pharmacy or Biological Sciences Several years of experience within medical devices surveillance, pharmacovigilance, or drug/device development; experience with in-vitro diagnostics or software as medical devices is seen as a bonus. A good understanding of medical concepts, disease processes, scientific methodology and data analysis. Proven track record with clinical trial activities and/or documented scientific training (e.g., PhD) will be an advantage. Fluent in English both written and spoken (company language) and an experienced user of MS Office. As a person, you uphold strong ethical values, demonstrate responsibility, and possess excellent organisational skills. You communicate effectively and efficiently, proving resilient under pressure and adept at navigating unforeseen challenges. Your collaborative nature and commitment to teamwork shine through, especially in a multicultural setting that emphasizes ongoing growth and development. Furthermore, you are good at establishing contact and collaborating with stakeholders. About the department Safety Surveillance is a distinguished department operating within the expansive framework of Global Safety, strategically headquartered in Soeborg, Denmark. Our global mandate is to assume responsibility for the comprehensive surveillance of safety-related information pertaining to all of Novo Nordisk's products, irrespective of whether they are presently in the market or in the developmental pipeline. We are entrusted with the critical task of safeguarding the well-being of individuals worldwide by closely monitoring the safety profiles of these products, ensuring they meet the highest standards of safety and efficacy throughout their lifecycle. Working at Novo Nordisk At Novo Nordisk, we don’t wait for change. We drive it. We’re 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 to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact Marcus Schartau, Manager at +45 3075 6713. Deadline 12 November 2023. We encourage you to apply as soon as possible, as the interviews will be conducted on an ongoing basis. You do not need to attach a cover letter to your application, but please include a few sentences about why you are applying in your resume or CV. 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 "Apoteker", og befinder sig i kategorien "Sundhed og forskning".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 24.10.2023, 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.
- Apoteker
- Søborg
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