Specialists within Safety Surveillance
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Søborg
Are you ready to embark on a career that empowers you to make a significant impact on the lives of thousands of people worldwide by ensuring highest safety and lowest possible risk to patients that use our products? Would you like to be part of high-profile projects within safety surveillance where your expertise and contributions are at the forefront of ensuring drug safety? We are looking for experienced Safety Surveillance Specialists who can drive projects and are eager to enhance their skills within the esteemed ranks of Novo Nordisk - a global leader in the pharmaceutical industry. Don’t wait, apply now for this exciting job opportunity! The position We are currently in the process of expanding our clinical activities and are seeking individuals to help lead a range of prestigious projects. We are actively searching for multiple highly competent Safety Surveillance Specialists who can join our team. As Safety Surveillance Specialist, you will play a pivotal role in supporting the safety surveillance of products in both clinical development stages II & III and for those already in the market. You will have the opportunity to work both independently and collaboratively with a team of highly skilled, committed, and enthusiastic colleagues. You will establish close partnership and interaction with other functional areas within Novo Nordisk, especially the Clinical Development and Regulatory Affairs teams, providing you with extensive insights into the entire Novo Nordisk value chain. Taking on responsibilities, sharing information, and taking proactive steps will be integral aspects of your daily tasks. Key responsibilities include: Contribute to development of new drugs by using your medical/clinical expertise on collection and assessment of safety information
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
Communicate information regarding the assessment of benefits and risks
Represent Safety Surveillance in cross-functional teams
Potentially chair the internal Novo Nordisk safety committee for one or more products
Qualifications As an ideal candidate, you have: University degree in Medicine, Veterinary Medicine, Pharmacy or Biological Sciences
Minimum 7 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. 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 additionally handle safety label updates, preparation of Risk Management Plans and aggregate reports. 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 either Cecilie Freddie Lange at +45 3079 4908, Kamilla Kjær Frederiksen at +45 3077 6794 or Nina Engberg Jungdal at +45 3079 9913. Deadline 15 October 2023. We encourage you to apply as soon as possible as candidates will be evaluated on an ongoing basis, and you may be contacted before the deadline. 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 "Forretningsudvikler", og befinder sig i kategorien "Kommunikation, marketing, salg".
Arbejdsstedet er beliggende i Søborg.
Jobbet er oprettet på vores service den 22.9.2023, 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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