Early Development and Rare Disease - experienced Safety Surveillance Advisers
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Søborg
Do you want to lead and drive safety surveillance activities in early phase development projects or in late phase projects in rare diseases? And would you like to be part of one of the most skilled and advanced pharmacovigilance functions in Denmark? We have open positions for experienced candidates in two Safety Surveillance teams at Novo Nordisk. Apply today for a life-changing career! About the Teams Safety Surveillance Early Development and Safety Surveillance Rare Disease are two teams within Global Safety at Novo Nordisk. Our dedicated and skilled professionals have global responsibility for the establishment of the product safety profile during clinical development, and for performing critical analysis and medical evaluation of the emerging aggregate safety data. Due to an increase in the number of development projects, our teams are expanding. In the Early Development team, we handle all First Human Dose (FHD) trials across all indications at Novo Nordisk. You will be the responsible safety surveillance lead for several development products from the early preparations for FHD, through phase 1 trial conduct and in the reporting phase. In the Rare Disease team, we handle projects within the rare disease indication from late phase development to post marketing. You will in collaboration with other colleagues in the team, be responsible for surveillance activities related to the compounds in development for rare blood disease indications. The Position Responsibilities may include: Chair cross-functional drug safety committees. Prepare communication about the benefit risk assessment. Contribute to development of clinical study designs and protocols. Communicate with external parties related to clinical safety monitoring such as Data Monitoring Committees. 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 across the functional areas in Novo Nordisk, especially the Non-clinical and Clinical Development teams. Assuming responsibility, communicating information and taking action will be essential parts of your workday. Qualifications As an ideal candidate, you will have: A Master’s degree within Medicine or Natural Sciences (MD, DVM, MSc Pharm or equivalent), preferably complemented by a PhD/research experience Several years of experience within pharmacovigilance, or from early phase development within the pharmaceutical industry and a strong desire to specialise within safety surveillance A solid understanding of medical concepts, scientific methodology, and drug development The ability to work independently as well as to collaborate in a continuous developing environment It is important that you are a strong collaborator who thrives in a multicultural environment of continuous development, and that you are good at establishing contacts and collaborating with stakeholders. As a person, you are self-driven and able to work independently and under pressure when needed. You are ethical, responsible, well-organised and a strong communicator. 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, through to manufacturing, marketing and sales – we’re all working to move the needle on patient care. Contact For further information, please contact: Safety Surveillance Early Development: Christine Dethlefsen at +45 30751225 Safety Surveillance Rare Disease: Michala Gauguin at +45 30793866 Deadline 05 November 2023. Applications will be reviewed on an ongoing basis, so we encourage you to apply as soon as possible. Please include a few sentences about why you are applying for the position in your resume or CV. You do not need to attach a cover letter to your application. To ensure an efficient and fair recruitment process, please refrain from adding a photo to your CV. We are looking for several Safety profiles at Novo Nordisk. Therefore, hiring Managers from different teams might also look at your application. Please indicate in your application if we are not allowed to share your application. 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 20.10.2023, 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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