Principal Scientist Safety Pharmacology
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Måløv
Are you passionate about drug effects on heart, brain and lung function? Do you wonder when drug effects on haemodynamics in animals can be a problem for patients? If yes, you may be the one, we are looking for. We are hiring an experienced non-clinical safety pharmacologist. Apply today! The Position As part of non-clinical project teams, your areas of responsibility will include:
• Building the suitable safety pharmacology package for new molecules across our portfolio.
• Study planning, study conduct, as well as study reporting in close collaboration with study directors at the Contract Research Organizations (CROs), internal principal investigators and other key stakeholders.
• Working closely with toxicologists when safety pharmacology endpoints are included in toxicity studies, and when general safety assessments are to be determined.
• Close collaboration with clinical projects’ members given that translation/safety assessment of the non-clinical safety pharmacology data is always the key question.
• Based on the collected project safety pharmacology data, we expect you to become the key driver in the safety assessment in your project teams, advancing the drug candidates towards the first clinical trials and writing the required documents to health authorities. Qualifications We expect you to have:
• A veterinary- or life science degree combined with a good understanding of physiology and normal laboratory animal behaviour.
• PhD within a relevant discipline will be an advantage, or otherwise proven skills in experimental work and scientific writing.
• experience with Good Laboratory Practice (GLP) compliant non-clinical in vitro and in vivo safety pharmacology studies from pharma, biotech or a CRO.
• Full proficiency in English, both written and spoken and you are capable of efficient communication and have good presentation skills.
• Experience in writing documents to health authorities.
As a person you have a strong scientific mind-set as this will be key in the interaction with internal as well external stakeholders. You are a thorough, energetic fast learner, you proactively take responsibility, and you find it valuable to invest in good and open collaborations and interactions with your colleagues fostering a positive work environment.
Novo Nordisk is a world leading pharmaceutical company and an international workplace used to onboard national as well as international employees. We welcome international candidates and will help with the relocation.
About the Department Currently we are 2 full time safety pharmacologists in the Department of Safety Pharmacology and Early Toxicology. We strive to follow the literature, new methods, and regulatory requirements within the field of safety pharmacology and prioritize knowledge sharing in general. To support our exciting and growing project portfolio which both compasses small and large molecules, we need you to grow our safety pharmacology team and capabilities. Our key task is to progress our development projects towards the first clinical trials with focus on high quality science, animal welfare including reducing animal use, project timelines and ultimately human safety.
Besides the safety pharmacology group, we have 6 great toxicology colleagues in the department and our department works closely together with our sister toxicology department supporting the entire development project portfolio. We have a long track record in running safety pharmacology studies at Contract Research Organizations (CROs) - and we also have a tradition for being contributors to the scientific community (speaking at conferences, writing publications, teaching at courses, and supporting the international Safety Pharmacology Society). Our department is characterized by an open, collaborative, and ambitious atmosphere and we work both from home and our modern open-office facilities located in Måløv, Denmark. Working at Novo Nordisk We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact For further information, please contact Principal Scientist, safety pharmacologist Ninette Kieme Andersen on +45 30756240
Deadline 19 February 2023. Applications will be reviewed on an ongoing basis, so you are encouraged to apply as soon as possible. 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.
• Building the suitable safety pharmacology package for new molecules across our portfolio.
• Study planning, study conduct, as well as study reporting in close collaboration with study directors at the Contract Research Organizations (CROs), internal principal investigators and other key stakeholders.
• Working closely with toxicologists when safety pharmacology endpoints are included in toxicity studies, and when general safety assessments are to be determined.
• Close collaboration with clinical projects’ members given that translation/safety assessment of the non-clinical safety pharmacology data is always the key question.
• Based on the collected project safety pharmacology data, we expect you to become the key driver in the safety assessment in your project teams, advancing the drug candidates towards the first clinical trials and writing the required documents to health authorities. Qualifications We expect you to have:
• A veterinary- or life science degree combined with a good understanding of physiology and normal laboratory animal behaviour.
• PhD within a relevant discipline will be an advantage, or otherwise proven skills in experimental work and scientific writing.
• experience with Good Laboratory Practice (GLP) compliant non-clinical in vitro and in vivo safety pharmacology studies from pharma, biotech or a CRO.
• Full proficiency in English, both written and spoken and you are capable of efficient communication and have good presentation skills.
• Experience in writing documents to health authorities.
As a person you have a strong scientific mind-set as this will be key in the interaction with internal as well external stakeholders. You are a thorough, energetic fast learner, you proactively take responsibility, and you find it valuable to invest in good and open collaborations and interactions with your colleagues fostering a positive work environment.
Novo Nordisk is a world leading pharmaceutical company and an international workplace used to onboard national as well as international employees. We welcome international candidates and will help with the relocation.
About the Department Currently we are 2 full time safety pharmacologists in the Department of Safety Pharmacology and Early Toxicology. We strive to follow the literature, new methods, and regulatory requirements within the field of safety pharmacology and prioritize knowledge sharing in general. To support our exciting and growing project portfolio which both compasses small and large molecules, we need you to grow our safety pharmacology team and capabilities. Our key task is to progress our development projects towards the first clinical trials with focus on high quality science, animal welfare including reducing animal use, project timelines and ultimately human safety.
Besides the safety pharmacology group, we have 6 great toxicology colleagues in the department and our department works closely together with our sister toxicology department supporting the entire development project portfolio. We have a long track record in running safety pharmacology studies at Contract Research Organizations (CROs) - and we also have a tradition for being contributors to the scientific community (speaking at conferences, writing publications, teaching at courses, and supporting the international Safety Pharmacology Society). Our department is characterized by an open, collaborative, and ambitious atmosphere and we work both from home and our modern open-office facilities located in Måløv, Denmark. Working at Novo Nordisk We are a proud life-science company, and life is our reason to exist. We’re inspired by life in all its forms and shapes, ups and downs, opportunities and challenges. For employees at Novo Nordisk, life means many things – from the building blocks of life that form the basis of ground-breaking scientific research, to our rich personal lives that motivate and energise us to perform our best at work. Ultimately, life is why we’re all here - to ensure that people can lead a life independent of chronic disease. Contact For further information, please contact Principal Scientist, safety pharmacologist Ninette Kieme Andersen on +45 30756240
Deadline 19 February 2023. Applications will be reviewed on an ongoing basis, so you are encouraged to apply as soon as possible. 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 Måløv.
Jobbet er oprettet på vores service den 30.1.2023, 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
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