Toxicologist/Principal Toxicologist, Non-Clinical Safety
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Måløv
Are you passionate about non-clinical safety assessment of compounds supporting the development of a growing pipeline at Novo Nordisk? Do you want to work in a dynamic and international environment making a difference for patients within diabetes, obesity, NASH, cardiovascular and other chronic diseases? Then you might be the Non-Clinical Safety Scientist/Toxicologist that we are looking for to join our passionate, dedicated and experienced team. The position
In this position, you will represent the department as a key member of multidisciplinary project teams, provide non-clinical safety assessments, and support and give input to the execution of Novo Nordisk´s non-clinical safety strategy. You will work independently as Sponsors Monitor on toxicology studies performed at CROs, in close collaboration with colleagues from manufacturing (CMC), Non-clinical Project Managers, Pathology, Bioanalysis, ADME and PK/PD. You will be responsible for the non-clinical safety studies primarily supporting first-human dose (FHD) according to relevant ICH guidelines. This position is on-site in Greater Copenhagen area, and we offer relocation support to international candidates.
Qualifications
You thrive in a dynamic milieu of coordinating complex tasks with a variety of stakeholders as sponsors monitor while planning, conducting, and overseeing studies performed at CROs. You timely deliver high-quality non-clinical safety evaluations to early-stage projects. To be considered for this position:
• You have a strong ability to analyse data, including toxicology, pharmacology and pharmaco-kinetic/-dynamic data
• Previous experience in drug development, with support of health authority interactions delivering non-clinical input to regulatory documents and meetings is preferred.
• You can effectively communicate complex data and findings with colleagues, teams, regulatory authorities and stakeholders
• You are passionate and persistent with a track-record of successfully managing pre-clinical pharmacology studies or toxicology projects
• You are fluent in written and spoken English
• You are curious on new ways of working and have an open mindset on how to solve your tasks
You will be part of a team in a highly dynamic environment, where both scientific and operational excellence will be expected. As a person you should have a scientific and objective mind-set, support our high ethical standards for animal studies, pro-actively solve tasks, be a team player, and have focus on quality and structure. You are curious to learn, energetic, and you take responsibility - but most importantly, you are eager to contribute to the common goals in the non-clinical area - Global Discovery & Development Sciences.
We encourage you to apply even if you don’t meet all the above requirements. About the department
The department Safety Pharmacology & Early Toxicology is a part of Global Discovery and Development Sciences, Novo Nordisk A/S located in Måløv and our main delivery is within non-clinical safety assessment. We are currently 10 experienced safety pharmacologists and toxicologists in the department, and we work closely together with our sister department Toxicology Development Projects. We need more hands to support the growing pipeline. We support the entire Novo Nordisk project portfolio including different modalities such as small molecules, peptides, monoclonal antibodies, proteins and siRNAs. 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
If you require further information, please contact Director, Peter Helding Kvist 30 79 75 88
Deadline
6 August 2023
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.
In this position, you will represent the department as a key member of multidisciplinary project teams, provide non-clinical safety assessments, and support and give input to the execution of Novo Nordisk´s non-clinical safety strategy. You will work independently as Sponsors Monitor on toxicology studies performed at CROs, in close collaboration with colleagues from manufacturing (CMC), Non-clinical Project Managers, Pathology, Bioanalysis, ADME and PK/PD. You will be responsible for the non-clinical safety studies primarily supporting first-human dose (FHD) according to relevant ICH guidelines. This position is on-site in Greater Copenhagen area, and we offer relocation support to international candidates.
Qualifications
You thrive in a dynamic milieu of coordinating complex tasks with a variety of stakeholders as sponsors monitor while planning, conducting, and overseeing studies performed at CROs. You timely deliver high-quality non-clinical safety evaluations to early-stage projects. To be considered for this position:
• You have a strong ability to analyse data, including toxicology, pharmacology and pharmaco-kinetic/-dynamic data
• Previous experience in drug development, with support of health authority interactions delivering non-clinical input to regulatory documents and meetings is preferred.
• You can effectively communicate complex data and findings with colleagues, teams, regulatory authorities and stakeholders
• You are passionate and persistent with a track-record of successfully managing pre-clinical pharmacology studies or toxicology projects
• You are fluent in written and spoken English
• You are curious on new ways of working and have an open mindset on how to solve your tasks
You will be part of a team in a highly dynamic environment, where both scientific and operational excellence will be expected. As a person you should have a scientific and objective mind-set, support our high ethical standards for animal studies, pro-actively solve tasks, be a team player, and have focus on quality and structure. You are curious to learn, energetic, and you take responsibility - but most importantly, you are eager to contribute to the common goals in the non-clinical area - Global Discovery & Development Sciences.
We encourage you to apply even if you don’t meet all the above requirements. About the department
The department Safety Pharmacology & Early Toxicology is a part of Global Discovery and Development Sciences, Novo Nordisk A/S located in Måløv and our main delivery is within non-clinical safety assessment. We are currently 10 experienced safety pharmacologists and toxicologists in the department, and we work closely together with our sister department Toxicology Development Projects. We need more hands to support the growing pipeline. We support the entire Novo Nordisk project portfolio including different modalities such as small molecules, peptides, monoclonal antibodies, proteins and siRNAs. 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
If you require further information, please contact Director, Peter Helding Kvist 30 79 75 88
Deadline
6 August 2023
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 Måløv.
Jobbet er oprettet på vores service den 15.5.2023, 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
- Måløv
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