Senior Toxicologist/Specialist, 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, cardio-renal and rare diseases? Are you curious about new ways of working and digital solutions? Then apply today and join our passionate, dedicated and experienced team of toxicologists and safety pharmacologists. 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 (Contract Research Organizations), 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. Moreover, you will work in a dynamic environment and timely deliver high-quality non-clinical safety evaluations to early-stage projects. Qualifications: To be considered for this position, you should fulfill some of the below requirements: Have a master’s degree in Pharmaceuticals, Biology, Veterinary Medicine or similar. Work systematically and have a strong ability to analyse data, including toxicology, pharmacology and pharmaco-kinetic/-dynamic data. Have previous experience in drug development, with support of health authority interactions delivering non-clinical input to regulatory documents and meetings. Preferably have experience with toxicologic assessment of small molecules. Can effectively communicate complex data and findings with colleagues, teams, regulatory authorities and stakeholders. Are passionate and persistent with a track-record of successfully managing toxicology projects. Are fluent in written and spoken English. Experience and passion for using and exploring digital solutions for improvement of workflows. 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 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. Please, submit your application even if you do not have all the above qualifications. 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 Peter Helding Kvist, Director at +45 30 79 75 88. Deadline 16 October 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 3.10.2023, 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.
- Forretningsudvikler
- Måløv
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Statistik over udbudte forretningsudviklere i Måløv over tid
| Dato | Alle jobs som forretningsudviklere |
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| 30. juni 2024 | 9 |
| 29. juni 2024 | 9 |
| 28. juni 2024 | 11 |
| 27. juni 2024 | 11 |
| 26. juni 2024 | 11 |
| 25. juni 2024 | 11 |
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| 16. juni 2024 | 12 |
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| 14. juni 2024 | 9 |
| 13. juni 2024 | 7 |
| 12. juni 2024 | 7 |
| 11. juni 2024 | 5 |
| 10. juni 2024 | 9 |
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| 4. juni 2024 | 15 |
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| 2. juni 2024 | 15 |
| 1. juni 2024 | 14 |
| 31. maj 2024 | 14 |