Principal Scientist, Non-clinical Safety
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Do you thrive in an environment with a high variety of tasks and stakeholders? Are you passionate about non-clinical safety assessments of compounds? Are you curious about new ways of working and digital solutions? If you are ready for a life-changing career, read on and apply today! We are looking for 2 talented individuals to join our Toxicology Centre of Excellence at Novo Nordisk. The Position
As a Toxicologist at Novo Nordisk, you will support our key deliverables: Study planning, monitoring during the in-life phase, and study reporting. This will be done in collaboration with study directors at CROs (Contract Research Organizations) and internal key stakeholders. Other responsibilities include: Overall planning of toxicology programs for drug development projects which we aim to design as lean as possible and yet adhere to regulatory guidelines from the International Conference on Harmonization (ICH) Authoring regulatory documents (INDs, CTAs, IBs, BLAs, etc.) as well as responding to questions from authorities Trying new ways of working and optimizing the way we work, both concerning science and operational efficiency Qualifications
You will be part of a team in a dynamic and challenging environment. Please submit your application even if you do not have all the above qualifications. To be successful in this role, we are looking for a candidate with the following qualifications: 5+ years of toxicological experience in the pharma industry Strong experience of toxicology and ICH guidelines Experience with in vitro assays or in silico analysis is an advantage Experience with experimental work/animal studies, either performing it yourself or at CROs Flair for analyzing and presenting scientific data both orally and in writing Capability to understand the biology of the target and interpret data Drive to take responsibility for your own projects Support for our high ethical standards for animal studies and consideration of using microphysiological systems and new approach methodologies when relevant As a person, you are proactive in contacting and communicating with stakeholders, adept at using networks. You have a flair for balancing several tasks with tight deadlines and delivering in adequate quality. Additionally, you possess the ability to train and support younger colleagues in their development. About the Department
The open positions are both within our Toxicology Centre of Excellence consisting of two departments: Safety Pharmacology & Early Toxicology and Toxicology Development Projects. We are part of Global Drug Discovery, and our main delivery is within non-clinical safety assessment. The departments work closely together and support the drug pipeline with toxicology studies leading up to first-in-man studies and the market, including general toxicology, genotoxicity, reproductive toxicity, and carcinogenicity studies. We support the entire Novo Nordisk project portfolio including small molecules, peptides, proteins, monoclonal antibodies, siRNA, and gene editing. We design toxicology programs and actively participate in multi-disciplinary non-clinical project teams (project manager, toxicology, bioanalysis, pharmacokinetics, ADME, pathology). The organization is global, and we collaborate closely with colleagues in the Boston area. The studies are performed at external contract research organizations (CROs) with whom we have a lot of scientific sparring and coordination of activities. We also propose and contribute to the investigative and mechanistic understanding of toxicities to evaluate human relevance. Currently, we are 20 scientists including safety pharmacologists, project toxicologists, and toxicologists looking into toxicology related to non-active ingredients such as excipients, impurities, or biocompatibility evaluation of devices. We have a high focus on science, animal welfare, and operational efficiency, all allowing optimizing and digitalizing the way we work. Our area is characterized by an open, sharing, collaborative, and ambitious atmosphere with good opportunities for further development. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive change. 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. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 61,000 employees around the world to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Peter Helding Kvist, Director of Safety Pharmacology & Early Toxicology at +4530797588 or Julie Mangor Lovmand, Director of Toxicology Development Projects at + 4530757879. Deadline 28 December 2023. We will do job interviews on a running basis. You do not need to attach a cover letter to your application – just include a few sentences about why you are applying in your CV. Please also avoid the use of photos in your CV. This makes for a better and less biased process. 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.
As a Toxicologist at Novo Nordisk, you will support our key deliverables: Study planning, monitoring during the in-life phase, and study reporting. This will be done in collaboration with study directors at CROs (Contract Research Organizations) and internal key stakeholders. Other responsibilities include:
You will be part of a team in a dynamic and challenging environment. Please submit your application even if you do not have all the above qualifications. To be successful in this role, we are looking for a candidate with the following qualifications:
The open positions are both within our Toxicology Centre of Excellence consisting of two departments: Safety Pharmacology & Early Toxicology and Toxicology Development Projects. We are part of Global Drug Discovery, and our main delivery is within non-clinical safety assessment. The departments work closely together and support the drug pipeline with toxicology studies leading up to first-in-man studies and the market, including general toxicology, genotoxicity, reproductive toxicity, and carcinogenicity studies. We support the entire Novo Nordisk project portfolio including small molecules, peptides, proteins, monoclonal antibodies, siRNA, and gene editing. We design toxicology programs and actively participate in multi-disciplinary non-clinical project teams (project manager, toxicology, bioanalysis, pharmacokinetics, ADME, pathology). The organization is global, and we collaborate closely with colleagues in the Boston area. The studies are performed at external contract research organizations (CROs) with whom we have a lot of scientific sparring and coordination of activities. We also propose and contribute to the investigative and mechanistic understanding of toxicities to evaluate human relevance. Currently, we are 20 scientists including safety pharmacologists, project toxicologists, and toxicologists looking into toxicology related to non-active ingredients such as excipients, impurities, or biocompatibility evaluation of devices. We have a high focus on science, animal welfare, and operational efficiency, all allowing optimizing and digitalizing the way we work. Our area is characterized by an open, sharing, collaborative, and ambitious atmosphere with good opportunities for further development. Working at Novo Nordisk
At Novo Nordisk, we don’t wait for change. We drive change. 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. Working at Novo Nordisk is working toward something bigger than ourselves, and it’s a collective effort. Novo Nordisk relies on the joint potential and collaboration of its more than 61,000 employees around the world to change the lives for the better for millions of patients living with diabetes and other chronic diseases. Together, we go further. Together, we’re life changing. Contact
For further information, please contact Peter Helding Kvist, Director of Safety Pharmacology & Early Toxicology at +4530797588 or Julie Mangor Lovmand, Director of Toxicology Development Projects at + 4530757879. Deadline 28 December 2023. We will do job interviews on a running basis. You do not need to attach a cover letter to your application – just include a few sentences about why you are applying in your CV. Please also avoid the use of photos in your CV. This makes for a better and less biased process. 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 Måløv.
Jobbet er oprettet på vores service den 12.12.2023, 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.
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